geneid | 348158 |
---|---|
ensemblid | ENSG00000066813.14 |
hgncid | 30931 |
symbol | ACSM2B |
name | acyl-CoA synthetase medium chain family member 2B |
refseq_nuc | NM_001105069.2 |
refseq_prot | NP_001098539.1 |
ensembl_nuc | ENST00000329697.10 |
ensembl_prot | ENSP00000327453.6 |
mane_status | MANE Select |
chr | chr16 |
start | 20536226 |
end | 20576367 |
strand | - |
ver | v1.2 |
region | chr16:20536226-20576367 |
region5000 | chr16:20531226-20581367 |
regionname0 | ACSM2B_chr16_20536226_20576367 |
regionname5000 | ACSM2B_chr16_20531226_20581367 |
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 | 0/1 | 577 | 253 | 25 | 59 | 124 | 12 | 32 | 95 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002 | 0/0 | 577 | 53 | 14 | 4 | 30 | 0 | 5 | 27 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003 | 0/0 | 577 | 22 | 18 | 1 | 0 | 0 | 3 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0004 | 0/0 | 577 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005 | 1/0 | 577 | 11 | 6 | 2 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006 | 0/0 | 577 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0007 | 0/0 | 577 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0008 | 0/0 | 577 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0009 | 0/0 | 577 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0010 | 0/0 | 577 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0011 | 0/0 | 577 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0012 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0013 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0014 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0015 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0016 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
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 | 99 | 0 | 10 | 80 | 4 | 5 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0002 | 0/1 | 1734 | 97 | 19 | 40 | 10 | 7 | 20 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0003 | 0/0 | 1734 | 37 | 13 | 3 | 19 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0004 | 0/0 | 1734 | 35 | 0 | 7 | 26 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0005 | 0/0 | 1734 | 19 | 17 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0006 | 0/0 | 1734 | 13 | 1 | 1 | 8 | 1 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0007 | 0/0 | 1734 | 11 | 9 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0008 | 0/0 | 1734 | 9 | 8 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0009 | 0/0 | 1734 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0010 | 0/0 | 1734 | 8 | 8 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0011 | 1/0 | 1734 | 7 | 3 | 2 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0012 | 0/0 | 1734 | 5 | 4 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0013 | 0/0 | 1734 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0014 | 0/0 | 1734 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0015 | 0/0 | 1734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0016 | 0/0 | 1734 | 3 | 2 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0017 | 0/0 | 1734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0018 | 0/0 | 1734 | 3 | 1 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0019 | 0/0 | 1734 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0020 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0021 | 0/0 | 1734 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0022 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0023 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0024 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0025 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0026 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0027 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0028 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0029 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0030 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0031 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0032 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
c0033 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
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 | 1/0 | 1202 | 79 | 1 | 8 | 57 | 5 | 7 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0002 | 0/0 | 1202 | 63 | 12 | 28 | 13 | 0 | 10 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0003 | 0/0 | 1202 | 55 | 21 | 4 | 28 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0004 | 0/0 | 1202 | 53 | 3 | 15 | 15 | 6 | 14 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0005 | 0/0 | 1202 | 30 | 6 | 2 | 20 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0006 | 0/0 | 1202 | 22 | 17 | 2 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0007 | 0/1 | 1202 | 21 | 7 | 3 | 8 | 1 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0008 | 0/0 | 1202 | 10 | 1 | 2 | 3 | 0 | 4 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0009 | 0/0 | 1202 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0010 | 0/0 | 1202 | 7 | 5 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0011 | 0/0 | 1202 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0012 | 0/0 | 1202 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0013 | 0/0 | 1202 | 4 | 3 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0014 | 0/0 | 1202 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0015 | 0/0 | 1198 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0016 | 0/0 | 1202 | 3 | 2 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0017 | 0/0 | 1202 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0018 | 0/0 | 1202 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0019 | 0/0 | 1202 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0020 | 0/0 | 1202 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0021 | 0/0 | 1202 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0022 | 0/0 | 1202 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0023 | 0/0 | 1202 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0024 | 0/0 | 1202 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0025 | 0/0 | 1202 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0026 | 0/0 | 1202 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0027 | 0/0 | 1202 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0028 | 0/0 | 1202 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
t0029 | 0/0 | 1190 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
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 | 6 | 0 | 0 | 6 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0003 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
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 | 99 | 0 | 10 | 80 | 4 | 5 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002 | 0/1 | 1734 | 97 | 19 | 40 | 10 | 7 | 20 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0004 | 0/0 | 1734 | 35 | 0 | 7 | 26 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0006 | 0/0 | 1734 | 13 | 1 | 1 | 8 | 1 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0012 | 0/0 | 1734 | 5 | 4 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0017 | 0/0 | 1734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0027 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0003 | 0/0 | 1734 | 37 | 13 | 3 | 19 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0009 | 0/0 | 1734 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0018 | 0/0 | 1734 | 3 | 1 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0019 | 0/0 | 1734 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0029 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0007 | 0/0 | 1734 | 11 | 9 | 1 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0008 | 0/0 | 1734 | 9 | 8 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0025 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0033 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0004c0005 | 0/0 | 1734 | 19 | 17 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0011 | 1/0 | 1734 | 7 | 3 | 2 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0016 | 0/0 | 1734 | 3 | 2 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0024 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0010 | 0/0 | 1734 | 8 | 8 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0020 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0007c0014 | 0/0 | 1734 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0008c0013 | 0/0 | 1734 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0009c0015 | 0/0 | 1734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0010c0022 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0010c0023 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0011c0021 | 0/0 | 1734 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0012c0030 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0013c0031 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0014c0026 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0015c0032 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0016c0028 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2935 | 63 | 0 | 7 | 48 | 4 | 4 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0001t0003 | 0/0 | 2935 | 27 | 0 | 3 | 24 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0001t0008 | 0/0 | 2935 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0001t0012 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0001t0018 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0001t0023 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0002 | 0/0 | 2935 | 36 | 7 | 20 | 1 | 0 | 8 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0003 | 0/0 | 2935 | 9 | 8 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0004 | 0/0 | 2935 | 42 | 3 | 15 | 8 | 6 | 10 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0007 | 0/1 | 2935 | 7 | 1 | 2 | 1 | 1 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0021 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0022 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0002t0024 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0004t0002 | 0/0 | 2935 | 21 | 0 | 7 | 12 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0004t0004 | 0/0 | 2935 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0004t0007 | 0/0 | 2935 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0006t0001 | 0/0 | 2935 | 8 | 0 | 1 | 4 | 1 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0006t0003 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0006t0011 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0012t0002 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0012t0007 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0017t0004 | 0/0 | 2935 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0001c0027t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0003t0005 | 0/0 | 2935 | 28 | 6 | 2 | 19 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0003t0010 | 0/0 | 2935 | 5 | 4 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0003t0013 | 0/0 | 2935 | 4 | 3 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0009t0009 | 0/0 | 2935 | 9 | 0 | 0 | 7 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0018t0005 | 0/0 | 2935 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0018t0010 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0019t0006 | 0/0 | 2935 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0002c0029t0010 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0007t0003 | 0/0 | 2935 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0007t0004 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0007t0007 | 0/0 | 2935 | 3 | 2 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0007t0014 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0008t0001 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0008t0003 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0008t0011 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0008t0015 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0025t0003 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0003c0033t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0004c0005t0006 | 0/0 | 2935 | 19 | 17 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0011t0001 | 1/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0011t0008 | 0/0 | 2935 | 3 | 0 | 2 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0011t0019 | 0/0 | 2935 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0011t0026 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0016t0016 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0016t0028 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0016t0029 | 0/0 | 2923 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0005c0024t0016 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0010t0003 | 0/0 | 2935 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0010t0017 | 0/0 | 2935 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0020t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0006c0020t0020 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0007c0014t0001 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0008c0013t0002 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0009c0015t0008 | 0/0 | 2935 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0010c0022t0008 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0010c0023t0027 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0011c0021t0001 | 0/0 | 2935 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0012c0030t0018 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0013c0031t0016 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0014c0026t0002 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0015c0032t0025 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
a0016c0028t0003 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | copy fasta | chr16 | 20531226 | 20581367 |
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 | 6 | 0 | 0 | 6 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0008g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0012g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0003 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0021g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0022g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0002t0024g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0004t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0006t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0012t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0017t0004g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0017t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0001c0027t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0003t0013g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0009t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0018t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0019t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0002c0029t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0007t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0015g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0008t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0025t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0003c0033t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0004c0005t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0001g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0008g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0019g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0011t0026g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0016g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0028g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0016t0029g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0005c0024t0016g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0017g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0010t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0020t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0006c0020t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0007c0014t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0008c0013t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0009c0015t0008g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0009c0015t0008g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0010c0022t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0010c0023t0027g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0011c0021t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0011c0021t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0012c0030t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0013c0031t0016g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0014c0026t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0015c0032t0025g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
a0016c0028t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0004 | g0276 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0267 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0303 | EUR | FIN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00423 | hp1 | a0015 | c0032 | t0025 | g0339 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00423 | hp2 | a0001 | c0004 | t0007 | g0020 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00438 | hp2 | a0001 | c0006 | t0001 | g0286 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00597 | hp2 | a0001 | c0004 | t0002 | g0144 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00609 | hp2 | a0001 | c0006 | t0003 | g0314 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00621 | hp2 | a0001 | c0004 | t0004 | g0021 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0308 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00639 | hp2 | a0001 | c0002 | t0007 | g0231 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0301 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00642 | hp2 | a0001 | c0002 | t0021 | g0269 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00673 | hp1 | a0002 | c0003 | t0005 | g0042 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00673 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | CHS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00733 | hp1 | a0001 | c0006 | t0001 | g0296 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00735 | hp2 | a0001 | c0004 | t0002 | g0175 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG00741 | hp2 | a0003 | c0007 | t0007 | g0229 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01074 | hp1 | a0001 | c0004 | t0002 | g0136 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01074 | hp2 | a0001 | c0012 | t0002 | g0245 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0262 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01099 | hp2 | a0004 | c0005 | t0006 | g0089 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0236 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0266 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01168 | hp1 | a0005 | c0011 | t0008 | g0330 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01168 | hp2 | a0001 | c0004 | t0002 | g0149 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01169 | hp1 | a0005 | c0011 | t0008 | g0331 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0259 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01175 | hp1 | a0001 | c0002 | t0004 | g0285 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0278 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01256 | hp1 | a0002 | c0029 | t0010 | g0080 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01256 | hp2 | a0001 | c0004 | t0002 | g0127 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01257 | hp1 | a0002 | c0003 | t0005 | g0078 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0238 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0251 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01346 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01361 | hp1 | a0001 | c0002 | t0007 | g0232 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0220 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0242 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0028 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01516 | hp1 | a0001 | c0006 | t0001 | g0289 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0028 | EUR | IBS | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01884 | hp1 | a0004 | c0005 | t0006 | g0087 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01884 | hp2 | a0006 | c0010 | t0017 | g0038 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01891 | hp1 | a0005 | c0011 | t0019 | g0033 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01891 | hp2 | a0002 | c0003 | t0005 | g0055 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0323 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01934 | hp2 | a0004 | c0005 | t0006 | g0096 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01943 | hp1 | a0002 | c0003 | t0013 | g0079 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01943 | hp2 | a0001 | c0004 | t0002 | g0143 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01952 | hp1 | a0001 | c0004 | t0002 | g0151 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01952 | hp2 | a0001 | c0002 | t0004 | g0274 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01975 | hp2 | a0002 | c0003 | t0005 | g0072 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01981 | hp1 | a0001 | c0002 | t0024 | g0272 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01981 | hp2 | a0001 | c0002 | t0004 | g0273 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0254 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0271 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02027 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02040 | hp1 | a0002 | c0003 | t0005 | g0077 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02055 | hp1 | a0003 | c0033 | t0003 | g0174 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02055 | hp2 | a0003 | c0007 | t0007 | g0322 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02056 | hp1 | a0001 | c0006 | t0003 | g0313 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02074 | hp1 | a0007 | c0014 | t0001 | g0200 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02074 | hp2 | a0002 | c0009 | t0009 | g0063 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02083 | hp2 | a0001 | c0002 | t0004 | g0312 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0283 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02145 | hp1 | a0002 | c0003 | t0013 | g0048 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02145 | hp2 | a0003 | c0008 | t0011 | g0321 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02148 | hp2 | a0001 | c0004 | t0002 | g0150 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0335 | EAS | CDX | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02155 | hp2 | a0001 | c0004 | t0007 | g0020 | EAS | CDX | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02257 | hp1 | a0008 | c0013 | t0002 | g0106 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02257 | hp2 | a0003 | c0008 | t0011 | g0316 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02258 | hp1 | a0004 | c0005 | t0006 | g0099 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02258 | hp2 | a0003 | c0007 | t0014 | g0340 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02280 | hp1 | a0006 | c0010 | t0003 | g0114 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0263 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0280 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02451 | hp1 | a0005 | c0016 | t0016 | g0326 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0261 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02572 | hp2 | a0004 | c0005 | t0006 | g0102 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02602 | hp1 | a0001 | c0002 | t0007 | g0221 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02602 | hp2 | a0001 | c0004 | t0002 | g0137 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02615 | hp1 | a0003 | c0008 | t0015 | g0318 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02615 | hp2 | a0006 | c0010 | t0003 | g0115 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02622 | hp1 | a0003 | c0007 | t0003 | g0240 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02622 | hp2 | a0004 | c0005 | t0006 | g0098 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02630 | hp1 | a0010 | c0022 | t0008 | g0325 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02630 | hp2 | a0010 | c0023 | t0027 | g0332 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02647 | hp2 | a0006 | c0010 | t0003 | g0117 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0265 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02698 | hp1 | a0001 | c0004 | t0002 | g0141 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02698 | hp2 | a0001 | c0017 | t0004 | g0026 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02717 | hp1 | a0014 | c0026 | t0002 | g0113 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02717 | hp2 | a0003 | c0007 | t0014 | g0342 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02723 | hp1 | a0004 | c0005 | t0006 | g0086 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02723 | hp2 | a0004 | c0005 | t0006 | g0093 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0287 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02738 | hp2 | a0005 | c0011 | t0008 | g0328 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02809 | hp1 | a0003 | c0008 | t0001 | g0319 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02809 | hp2 | a0002 | c0003 | t0005 | g0082 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02818 | hp1 | a0004 | c0005 | t0006 | g0095 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02818 | hp2 | a0001 | c0027 | t0003 | g0282 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02886 | hp1 | a0002 | c0003 | t0005 | g0084 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02886 | hp2 | a0008 | c0013 | t0002 | g0109 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02895 | hp1 | a0006 | c0010 | t0003 | g0011 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02896 | hp1 | a0003 | c0008 | t0015 | g0031 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02896 | hp2 | a0008 | c0013 | t0002 | g0107 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02897 | hp1 | a0003 | c0008 | t0015 | g0031 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02897 | hp2 | a0006 | c0010 | t0003 | g0011 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02922 | hp1 | a0005 | c0024 | t0016 | g0334 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02922 | hp2 | a0006 | c0010 | t0017 | g0037 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02965 | hp1 | a0001 | c0012 | t0007 | g0024 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02970 | hp1 | a0001 | c0012 | t0007 | g0223 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02970 | hp2 | a0002 | c0018 | t0010 | g0039 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02976 | hp1 | a0004 | c0005 | t0006 | g0103 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02976 | hp2 | a0002 | c0003 | t0005 | g0043 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0304 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03017 | hp2 | a0003 | c0007 | t0004 | g0310 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03098 | hp1 | a0016 | c0028 | t0003 | g0118 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03098 | hp2 | a0004 | c0005 | t0006 | g0100 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03130 | hp1 | a0003 | c0008 | t0011 | g0320 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03130 | hp2 | a0003 | c0007 | t0014 | g0343 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03139 | hp1 | a0003 | c0008 | t0011 | g0317 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03139 | hp2 | a0004 | c0005 | t0006 | g0094 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03195 | hp1 | a0002 | c0003 | t0005 | g0081 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0239 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03209 | hp1 | a0006 | c0020 | t0003 | g0105 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03209 | hp2 | a0004 | c0005 | t0006 | g0091 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03225 | hp1 | a0001 | c0012 | t0007 | g0024 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03225 | hp2 | a0002 | c0003 | t0010 | g0004 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0243 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03239 | hp2 | a0001 | c0002 | t0004 | g0275 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03453 | hp1 | a0008 | c0013 | t0002 | g0108 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03453 | hp2 | a0002 | c0003 | t0013 | g0047 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03486 | hp1 | a0001 | c0006 | t0011 | g0110 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03486 | hp2 | a0002 | c0003 | t0005 | g0050 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03490 | hp1 | a0001 | c0017 | t0004 | g0026 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03490 | hp2 | a0009 | c0015 | t0008 | g0032 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03491 | hp1 | a0002 | c0009 | t0009 | g0010 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03491 | hp2 | a0002 | c0003 | t0010 | g0053 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03492 | hp1 | a0002 | c0009 | t0009 | g0010 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03492 | hp2 | a0009 | c0015 | t0008 | g0032 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03516 | hp1 | a0003 | c0007 | t0007 | g0281 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | ESN | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03540 | hp1 | a0004 | c0005 | t0006 | g0092 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03540 | hp2 | a0005 | c0011 | t0026 | g0327 | AFR | GWD | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03579 | hp1 | a0006 | c0020 | t0020 | g0034 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03654 | hp2 | a0001 | c0002 | t0004 | g0027 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0291 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03688 | hp1 | a0001 | c0002 | t0004 | g0227 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03688 | hp2 | a0001 | c0006 | t0001 | g0292 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03704 | hp1 | a0003 | c0025 | t0003 | g0121 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0305 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03710 | hp1 | a0001 | c0006 | t0001 | g0299 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03710 | hp2 | a0002 | c0018 | t0005 | g0075 | SAS | PJL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03831 | hp1 | a0011 | c0021 | t0001 | g0193 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03831 | hp2 | a0002 | c0003 | t0005 | g0059 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0290 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03834 | hp2 | a0001 | c0017 | t0004 | g0268 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03927 | hp1 | a0003 | c0008 | t0003 | g0122 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03927 | hp2 | a0009 | c0015 | t0008 | g0329 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03942 | hp1 | a0001 | c0001 | t0023 | g0208 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0247 | SAS | BEB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04115 | hp1 | a0001 | c0002 | t0004 | g0298 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04115 | hp2 | a0001 | c0002 | t0022 | g0309 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04199 | hp2 | a0005 | c0016 | t0029 | g0324 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0288 | SAS | STU | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18522 | hp2 | a0003 | c0007 | t0014 | g0341 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18612 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | CHB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0337 | EAS | CHB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18906 | hp1 | a0005 | c0016 | t0028 | g0333 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18906 | hp2 | a0004 | c0005 | t0006 | g0097 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18939 | hp1 | a0002 | c0003 | t0005 | g0085 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18942 | hp1 | a0002 | c0003 | t0005 | g0009 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18943 | hp1 | a0001 | c0004 | t0007 | g0217 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18943 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18945 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18946 | hp1 | a0001 | c0004 | t0004 | g0215 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18946 | hp2 | a0002 | c0003 | t0005 | g0009 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18947 | hp1 | a0012 | c0030 | t0018 | g0139 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18948 | hp1 | a0002 | c0009 | t0009 | g0061 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18951 | hp1 | a0001 | c0004 | t0004 | g0199 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18953 | hp1 | a0001 | c0001 | t0012 | g0035 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18953 | hp2 | a0007 | c0014 | t0001 | g0155 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18954 | hp1 | a0002 | c0003 | t0005 | g0074 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18956 | hp2 | a0002 | c0003 | t0005 | g0056 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18957 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18957 | hp2 | a0001 | c0004 | t0007 | g0202 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18959 | hp1 | a0002 | c0003 | t0005 | g0044 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18959 | hp2 | a0002 | c0009 | t0009 | g0073 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18961 | hp1 | a0001 | c0006 | t0003 | g0225 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18961 | hp2 | a0001 | c0004 | t0007 | g0203 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18964 | hp2 | a0001 | c0002 | t0004 | g0297 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18966 | hp2 | a0001 | c0004 | t0002 | g0128 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18967 | hp1 | a0001 | c0004 | t0004 | g0185 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18967 | hp2 | a0002 | c0009 | t0009 | g0057 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18968 | hp2 | a0002 | c0003 | t0005 | g0065 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18973 | hp2 | a0001 | c0004 | t0002 | g0133 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18974 | hp1 | a0002 | c0003 | t0005 | g0068 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18974 | hp2 | a0002 | c0009 | t0009 | g0076 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18975 | hp1 | a0001 | c0004 | t0002 | g0189 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18977 | hp1 | a0001 | c0006 | t0003 | g0226 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18978 | hp1 | a0002 | c0003 | t0005 | g0060 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18982 | hp1 | a0001 | c0004 | t0002 | g0188 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0270 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18988 | hp1 | a0002 | c0019 | t0006 | g0067 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18990 | hp2 | a0001 | c0006 | t0001 | g0307 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18992 | hp1 | a0001 | c0004 | t0002 | g0130 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18994 | hp1 | a0002 | c0003 | t0005 | g0066 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18997 | hp1 | a0007 | c0014 | t0001 | g0166 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19001 | hp1 | a0001 | c0004 | t0002 | g0126 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19004 | hp1 | a0001 | c0004 | t0004 | g0186 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19005 | hp1 | a0002 | c0003 | t0005 | g0046 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19005 | hp2 | a0001 | c0001 | t0018 | g0138 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19006 | hp1 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19007 | hp1 | a0001 | c0004 | t0007 | g0016 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19007 | hp2 | a0001 | c0006 | t0001 | g0293 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19009 | hp1 | a0001 | c0004 | t0004 | g0209 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19010 | hp1 | a0002 | c0003 | t0005 | g0041 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19012 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19043 | hp1 | a0001 | c0002 | t0007 | g0104 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19043 | hp2 | a0004 | c0005 | t0006 | g0088 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19054 | hp1 | a0002 | c0003 | t0005 | g0051 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19056 | hp1 | a0002 | c0009 | t0009 | g0062 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19056 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19062 | hp1 | a0001 | c0004 | t0002 | g0129 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19062 | hp2 | a0002 | c0019 | t0006 | g0090 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19064 | hp1 | a0011 | c0021 | t0001 | g0194 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19067 | hp1 | a0001 | c0004 | t0007 | g0016 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19070 | hp1 | a0002 | c0003 | t0005 | g0069 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19072 | hp2 | a0002 | c0003 | t0005 | g0058 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19074 | hp1 | a0007 | c0014 | t0001 | g0213 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19077 | hp2 | a0002 | c0003 | t0005 | g0064 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19079 | hp2 | a0013 | c0031 | t0016 | g0338 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19081 | hp1 | a0002 | c0018 | t0005 | g0071 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19081 | hp2 | a0001 | c0006 | t0001 | g0306 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19083 | hp1 | a0002 | c0009 | t0009 | g0054 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19083 | hp2 | a0001 | c0002 | t0007 | g0294 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0336 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19084 | hp2 | a0001 | c0004 | t0002 | g0187 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19088 | hp2 | a0002 | c0019 | t0006 | g0070 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19091 | hp2 | a0002 | c0003 | t0005 | g0052 | EAS | JPT | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19240 | hp1 | a0005 | c0011 | t0019 | g0033 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA19240 | hp2 | a0001 | c0012 | t0007 | g0284 | AFR | YRI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20129 | hp1 | a0004 | c0005 | t0006 | g0045 | AFR | ASW | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | ASW | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0277 | EUR | TSI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20752 | hp2 | a0001 | c0002 | t0007 | g0230 | EUR | TSI | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0228 | SAS | GIH | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0300 | SAS | GIH | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0279 | AMR | CLM | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02109 | hp1 | a0006 | c0010 | t0003 | g0116 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02486 | hp1 | a0002 | c0003 | t0013 | g0049 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02486 | hp2 | a0003 | c0007 | t0003 | g0119 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02559 | hp1 | a0002 | c0003 | t0010 | g0083 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG02559 | hp2 | a0002 | c0003 | t0010 | g0004 | AFR | ACB | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03471 | hp1 | a0003 | c0007 | t0003 | g0120 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG03471 | hp2 | a0004 | c0005 | t0006 | g0101 | AFR | MSL | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG06807 | hp1 | a0004 | c0005 | t0006 | g0040 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20300 | hp1 | a0002 | c0003 | t0010 | g0004 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0260 | AFR | USA | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0027 | AFR | LWK | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0007 | g0224 | REF | REF | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
homoSapiens_grch38 | hp1 | a0005 | c0011 | t0001 | g0252 | REF | REF | ACSM2B_chr16_20531226_20581367 | ACSM2B | chr16 | 20531226 | 20581367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20537269
|
G | C | 1 | a0014 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1723C>G | p.Arg575Gly | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 1892/2935 | 1723/1734 | 575/577 | chr16 | 20537269 | ||
chr16:20540654
|
C | G | 1 | a0011 | 2 | HG03831.hp1 NA19064.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1629G>C | p.Lys543Asn | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1798/2935 | 1629/1734 | 543/577 | chr16 | 20540654 | ||
chr16:20540692
|
C | A | 1 | a0013 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1591G>T | p.Val531Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1760/2935 | 1591/1734 | 531/577 | chr16 | 20540692 | ||
chr16:20540766
|
T | C | 1 | a0015 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1517A>G | p.Lys506Arg | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1686/2935 | 1517/1734 | 506/577 | chr16 | 20540766 | ||
chr16:20542973
|
T | C | 1 | a0008 | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.1450A>G | p.Lys484Glu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1619/2935 | 1450/1734 | 484/577 | chr16 | 20542973 | ||
chr16:20543238
|
T | A | 1 | a0007 | 4 | HG02074.hp1 NA18953.hp2 NA18997.hp1 others(1): Show |
missense_variant | MODERATE | c.1306A>T | p.Asn436Tyr | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1475/2935 | 1306/1734 | 436/577 | chr16 | 20543238 | ||
chr16:20543260
|
T | G | 6 | a0003a0004a0006others(3): Show | 58 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(55): Show |
missense_variant&splice_region_variant | MODERATE | c.1284A>C | p.Glu428Asp | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1453/2935 | 1284/1734 | 428/577 | chr16 | 20543260 | ||
chr16:20545228
|
G | A | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1210C>T | p.Pro404Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/14 | 1379/2935 | 1210/1734 | 404/577 | chr16 | 20545228 | ||
chr16:20548455
|
T | C | 2 | a0006a0008 | 14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
missense_variant | MODERATE | c.913A>G | p.Ile305Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/14 | 1082/2935 | 913/1734 | 305/577 | chr16 | 20548455 | ||
chr16:20552206
|
T | C | 2 | a0002a0004 | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
missense_variant | MODERATE | c.832A>G | p.Thr278Ala | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/14 | 1001/2935 | 832/1734 | 278/577 | chr16 | 20552206 | ||
chr16:20559267
|
A | T | 1 | a0012 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.358T>A | p.Trp120Arg | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 527/2935 | 358/1734 | 120/577 | chr16 | 20559267 | ||
chr16:20559339
|
T | C | 14 | a0001a0002a0003others(11): Show | 375 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(372): Show |
missense_variant | MODERATE | c.286A>G | p.Ile96Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 455/2935 | 286/1734 | 96/577 | chr16 | 20559339 | ||
chr16:20559434
|
A | G | 1 | a0009 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.191T>C | p.Leu64Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 360/2935 | 191/1734 | 64/577 | chr16 | 20559434 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20540717
|
C | T | 1 | a0002c0029 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1566G>A | p.Gln522Gln | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1735/2935 | 1566/1734 | 522/577 | chr16 | 20540717 | ||
chr16:20540744
|
C | T | 1 | a0001c0012 | 5 | HG01074.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.1539G>A | p.Ser513Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1708/2935 | 1539/1734 | 513/577 | chr16 | 20540744 | ||
chr16:20540753
|
G | T | 20 | a0001c0002a0001c0004a0001c0012others(17): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
synonymous_variant | LOW | c.1530C>A | p.Ile510Ile | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/14 | 1699/2935 | 1530/1734 | 510/577 | chr16 | 20540753 | ||
chr16:20542926
|
G | A | 4 | a0002c0003a0002c0009a0002c0019others(1): Show | 50 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(47): Show |
synonymous_variant | LOW | c.1497C>T | p.Pro499Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1666/2935 | 1497/1734 | 499/577 | chr16 | 20542926 | ||
chr16:20542983
|
A | G | 1 | a0003c0033 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1440T>C | p.Asn480Asn | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/14 | 1609/2935 | 1440/1734 | 480/577 | chr16 | 20542983 | ||
chr16:20543215
|
G | A | 1 | a0001c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1329C>T | p.Leu443Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/14 | 1498/2935 | 1329/1734 | 443/577 | chr16 | 20543215 | ||
chr16:20546409
|
G | A | 1 | a0005c0024 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1164C>T | p.Ser388Ser | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/14 | 1333/2935 | 1164/1734 | 388/577 | chr16 | 20546409 | ||
chr16:20546469
|
T | C | 1 | a0016c0028 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1104A>G | p.Leu368Leu | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/14 | 1273/2935 | 1104/1734 | 368/577 | chr16 | 20546469 | ||
chr16:20548432
|
A | G | 2 | a0001c0017a0006c0010 | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
synonymous_variant | LOW | c.936T>C | p.Pro312Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/14 | 1105/2935 | 936/1734 | 312/577 | chr16 | 20548432 | ||
chr16:20555301
|
G | A | 1 | a0002c0019 | 3 | NA18988.hp1 NA19062.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.564C>T | p.Cys188Cys | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/14 | 733/2935 | 564/1734 | 188/577 | chr16 | 20555301 | ||
chr16:20559274
|
A | T | 1 | a0003c0025 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.351T>A | p.Pro117Pro | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/14 | 520/2935 | 351/1734 | 117/577 | chr16 | 20559274 | ||
chr16:20564726
|
C | A | 8 | a0001c0001a0001c0004a0003c0033others(5): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
synonymous_variant | LOW | c.120G>T | p.Val40Val | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/14 | 289/2935 | 120/1734 | 40/577 | chr16 | 20564726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20536326
|
T | G | 1 | a0001c0002t0021 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 932 | chr16 | 20536326 | |||||
chr16:20536472
|
G | A | 19 | a0001c0002t0002a0001c0002t0004a0001c0002t0021others(16): Show | 133 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 786 | chr16 | 20536472 | |||||
chr16:20536516
|
C | T | 1 | a0010c0023t0027 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*742G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 742 | chr16 | 20536516 | |||||
chr16:20536640
|
C | G | 1 | a0005c0011t0026 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 618 | chr16 | 20536640 | |||||
chr16:20536686
|
C | T | 2 | a0001c0001t0018a0012c0030t0018 | 2 | NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*572G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 572 | chr16 | 20536686 | |||||
chr16:20536753
|
C | A | 2 | a0001c0006t0011a0003c0008t0011 | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*505G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 505 | chr16 | 20536753 | |||||
chr16:20536768
|
CCTTTCTC others(5): Show |
C | 1 | a0005c0016t0029 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478_*489delAGAGGG others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 478 | chr16 | 20536768 | |||||
chr16:20536791
|
CTCTT | C | 1 | a0003c0008t0015 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*463_*466delAAGA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 463 | chr16 | 20536791 | |||||
chr16:20536804
|
G | A | 1 | a0001c0001t0023 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 454 | chr16 | 20536804 | |||||
chr16:20536838
|
C | T | 1 | a0001c0002t0022 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 420 | chr16 | 20536838 | |||||
chr16:20536929
|
C | T | 8 | a0001c0002t0004a0001c0002t0021a0001c0002t0024others(5): Show | 60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*329G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 329 | chr16 | 20536929 | |||||
chr16:20536958
|
G | A | 8 | a0001c0002t0007a0001c0004t0007a0001c0012t0007others(5): Show | 53 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*300C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 300 | chr16 | 20536958 | |||||
chr16:20537012
|
C | T | 54 | a0001c0001t0003a0001c0001t0008a0001c0001t0018others(51): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*246G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 246 | chr16 | 20537012 | |||||
chr16:20537112
|
T | G | 2 | a0001c0006t0011a0003c0008t0011 | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*146A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 146 | chr16 | 20537112 | |||||
chr16:20537114
|
T | C | 1 | a0001c0002t0024 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 14/14 | 144 | chr16 | 20537114 | |||||
chr16:20576235
|
G | A | 1 | a0003c0007t0014 | 4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-37C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11390 | chr16 | 20576235 | |||||
chr16:20576246
|
C | T | 9 | a0002c0003t0005a0002c0003t0010a0002c0003t0013others(6): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11401 | chr16 | 20576246 | |||||
chr16:20576286
|
C | T | 1 | a0006c0010t0017 | 2 | HG01884.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11441 | chr16 | 20576286 | |||||
chr16:20576338
|
A | G | 1 | a0001c0001t0012 | 4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-140T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11493 | chr16 | 20576338 | |||||
chr16:20576344
|
G | A | 14 | a0001c0001t0008a0003c0007t0014a0005c0011t0008others(11): Show | 24 | HG00423.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | chr16 | 20576344 | ||||||
chr16:20576347
|
A | G | 1 | a0006c0020t0020 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/14 | 11502 | chr16 | 20576347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20537475
|
T | C | 2 | a0002c0003t0005g0050a0005c0016t0028g0333 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1630-113A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537475 | ||||||
chr16:20537502
|
A | G | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-140T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537502 | ||||||
chr16:20537532
|
G | C | 2 | a0002c0003t0010g0083a0005c0024t0016g0334 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1630-170C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537532 | ||||||
chr16:20537562
|
G | C | 3 | a0001c0002t0002g0111a0005c0016t0016g0326a0014c0026t0002g0113 | 3 | HG02451.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1630-200C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537562 | ||||||
chr16:20537572
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1630-210G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537572 | ||||||
chr16:20537684
|
C | T | 27 | a0001c0002t0003g0012a0001c0002t0003g0112a0001c0002t0003g0262others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-322G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537684 | ||||||
chr16:20537771
|
C | A | 1 | a0005c0011t0026g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1630-409G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537771 | ||||||
chr16:20537785
|
C | T | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1630-423G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537785 | ||||||
chr16:20537808
|
T | G | 39 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(36): Show | 45 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1630-446A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537808 | ||||||
chr16:20537827
|
G | C | 1 | a0002c0009t0009g0061 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1630-465C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537827 | ||||||
chr16:20537853
|
T | A | 1 | a0010c0023t0027g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1630-491A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537853 | ||||||
chr16:20537884
|
A | G | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1630-522T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537884 | ||||||
chr16:20537949
|
TA | T | 3 | a0001c0012t0007g0024a0001c0012t0007g0223a0001c0012t0007g0284 | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-588delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537949 | ||||||
chr16:20537950
|
A | C | 43 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(40): Show | 49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1630-588T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537950 | ||||||
chr16:20537987
|
G | A | 37 | a0001c0002t0003g0012a0001c0002t0003g0029a0001c0002t0003g0112others(34): Show | 39 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1630-625C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20537987 | ||||||
chr16:20538067
|
C | T | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-705G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538067 | ||||||
chr16:20538102
|
T | C | 2 | a0001c0004t0007g0217a0002c0018t0005g0071 | 2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1630-740A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538102 | ||||||
chr16:20538141
|
G | C | 1 | a0001c0004t0002g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1630-779C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538141 | ||||||
chr16:20538183
|
G | A | 263 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(260): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1630-821C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538183 | ||||||
chr16:20538266
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1630-904T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538266 | ||||||
chr16:20538266
|
A | T | 2 | a0001c0002t0003g0112a0004c0005t0006g0089 | 2 | HG01099.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1630-904T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538266 | ||||||
chr16:20538272
|
T | C | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-910A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538272 | ||||||
chr16:20538300
|
G | A | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1630-938C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538300 | ||||||
chr16:20538455
|
G | A | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1630-1093C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538455 | ||||||
chr16:20538458
|
C | A | 1 | a0002c0009t0009g0010 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1630-1096G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538458 | ||||||
chr16:20538580
|
G | T | 7 | a0001c0002t0003g0029a0001c0027t0003g0282a0003c0007t0014g0340others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1630-1218C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538580 | ||||||
chr16:20538582
|
G | T | 1 | a0001c0006t0001g0293 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630-1220C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538582 | ||||||
chr16:20538588
|
G | A | 50 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(47): Show | 56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1630-1226C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538588 | ||||||
chr16:20538695
|
C | T | 3 | a0001c0002t0004g0027a0001c0002t0004g0275a0001c0002t0004g0279 | 4 | HG01123.hp2 HG03239.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-1333G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538695 | ||||||
chr16:20538726
|
T | C | 1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1630-1364A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538726 | ||||||
chr16:20538734
|
C | T | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1630-1372G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538734 | ||||||
chr16:20538778
|
G | A | 119 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(116): Show | 133 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1630-1416C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538778 | ||||||
chr16:20538808
|
A | G | 1 | a0002c0003t0005g0064 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1630-1446T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538808 | ||||||
chr16:20538933
|
C | T | 1 | a0001c0004t0002g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1630-1571G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20538933 | ||||||
chr16:20539019
|
T | C | 1 | a0004c0005t0006g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1629+1635A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539019 | ||||||
chr16:20539025
|
C | T | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+1629G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539025 | ||||||
chr16:20539042
|
C | G | 176 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(173): Show | 195 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1629+1612G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539042 | ||||||
chr16:20539162
|
C | T | 1 | a0002c0009t0009g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1629+1492G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539162 | ||||||
chr16:20539288
|
ACCTATGA others(7): Show |
A | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+1352_1629+136 others(18): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539288 | ||||||
chr16:20539291
|
T | A | 3 | a0002c0003t0005g0081a0002c0003t0005g0082a0002c0003t0005g0084 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1629+1363A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539291 | ||||||
chr16:20539291
|
T | C | 2 | a0001c0004t0002g0126a0001c0004t0002g0130 | 2 | NA18992.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1629+1363A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539291 | ||||||
chr16:20539301
|
AG | A | 169 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(166): Show | 187 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1629+1352delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539301 | ||||||
chr16:20539302
|
G | C | 80 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(77): Show | 88 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1629+1352C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539302 | ||||||
chr16:20539305
|
T | C | 176 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(173): Show | 195 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1629+1349A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539305 | ||||||
chr16:20539393
|
G | A | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1629+1261C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539393 | ||||||
chr16:20539399
|
A | AT | 262 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(259): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.1629+1254dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539399 | ||||||
chr16:20539399
|
A | T | 1 | a0001c0002t0004g0278 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1629+1255T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539399 | ||||||
chr16:20539567
|
G | A | 1 | a0005c0011t0019g0033 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1629+1087C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539567 | ||||||
chr16:20539604
|
G | C | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+1050C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539604 | ||||||
chr16:20539721
|
G | A | 1 | a0003c0007t0014g0342 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1629+933C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539721 | ||||||
chr16:20539823
|
C | T | 120 | a0001c0001t0001g0179a0001c0002t0002g0007a0001c0002t0002g0025others(117): Show | 134 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1629+831G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539823 | ||||||
chr16:20539900
|
C | A | 43 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(40): Show | 49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+754G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539900 | ||||||
chr16:20539929
|
T | C | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+725A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539929 | ||||||
chr16:20539957
|
A | T | 50 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(47): Show | 56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1629+697T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20539957 | ||||||
chr16:20540014
|
T | A | 43 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(40): Show | 49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+640A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540014 | ||||||
chr16:20540109
|
A | G | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+545T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540109 | ||||||
chr16:20540176
|
A | G | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1629+478T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540176 | ||||||
chr16:20540209
|
A | C | 1 | a0001c0006t0011g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1629+445T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540209 | ||||||
chr16:20540213
|
G | T | 2 | a0003c0008t0011g0320a0003c0008t0011g0321 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1629+441C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540213 | ||||||
chr16:20540213
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0012g0008a0001c0001t0012g0036 | 3 | NA18957.hp1 NA19006.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1629+428_1629+440d others(15): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540213 | ||||||
chr16:20540224
|
G | GT | 60 | a0001c0001t0001g0168a0001c0002t0002g0233a0001c0002t0002g0234others(57): Show | 65 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1629+429dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540224 | ||||||
chr16:20540224
|
GT | G | 51 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(48): Show | 58 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1629+429delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540224 | ||||||
chr16:20540226
|
T | G | 43 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(40): Show | 49 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1629+428A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540226 | ||||||
chr16:20540231
|
T | G | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1629+423A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540231 | ||||||
chr16:20540233
|
T | G | 12 | a0001c0002t0003g0029a0001c0002t0003g0260a0001c0002t0003g0261others(9): Show | 13 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1629+421A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | ||||||
chr16:20540233
|
T | TG | 61 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(58): Show | 67 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1629+420_1629+421i others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | ||||||
chr16:20540233
|
T | TTG | 55 | a0001c0002t0002g0111a0001c0002t0004g0003a0001c0002t0004g0027others(52): Show | 63 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1629+420_1629+421i others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540233 | ||||||
chr16:20540246
|
T | G | 1 | a0001c0004t0004g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1629+408A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540246 | ||||||
chr16:20540250
|
G | GT | 62 | a0001c0001t0003g0181a0001c0002t0002g0111a0001c0002t0002g0233others(59): Show | 70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1629+403dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540250 | ||||||
chr16:20540250
|
G | T | 1 | a0001c0001t0012g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1629+404C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540250 | ||||||
chr16:20540284
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+370A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540284 | ||||||
chr16:20540286
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+368T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540286 | ||||||
chr16:20540292
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629+362C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540292 | ||||||
chr16:20540324
|
C | T | 1 | a0001c0002t0021g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1629+330G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540324 | ||||||
chr16:20540327
|
A | C | 1 | a0005c0011t0026g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1629+327T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540327 | ||||||
chr16:20540383
|
C | T | 45 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(42): Show | 51 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1629+271G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540383 | ||||||
chr16:20540386
|
G | A | 27 | a0001c0002t0004g0030a0001c0002t0004g0227a0001c0002t0004g0267others(24): Show | 29 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1629+268C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540386 | ||||||
chr16:20540463
|
G | C | 1 | a0001c0002t0004g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1629+191C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540463 | ||||||
chr16:20540502
|
C | T | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1629+152G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540502 | ||||||
chr16:20540519
|
A | G | 1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1629+135T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540519 | ||||||
chr16:20540533
|
A | G | 267 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(264): Show | 296 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.1629+121T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540533 | ||||||
chr16:20540637
|
G | C | 2 | a0001c0004t0002g0126a0001c0004t0002g0130 | 2 | NA18992.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1629+17C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 13/13 | chr16 | 20540637 | ||||||
chr16:20540782
|
T | C | 25 | a0001c0002t0003g0012a0001c0002t0003g0112a0001c0002t0003g0262others(22): Show | 26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-9A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540782 | ||||||
chr16:20540800
|
T | G | 1 | a0005c0011t0026g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1510-27A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540800 | ||||||
chr16:20540862
|
C | T | 42 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(39): Show | 48 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1510-89G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20540862 | ||||||
chr16:20541012
|
C | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1510-239G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541012 | ||||||
chr16:20541018
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA19001.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1510-245G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541018 | ||||||
chr16:20541071
|
G | A | 3 | a0001c0002t0003g0260a0001c0002t0003g0261a0001c0002t0003g0263 | 3 | HG02280.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1510-298C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541071 | ||||||
chr16:20541127
|
G | A | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1510-354C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541127 | ||||||
chr16:20541140
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1510-367C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541140 | ||||||
chr16:20541144
|
A | G | 48 | a0001c0002t0007g0221a0001c0002t0007g0224a0001c0002t0007g0230others(45): Show | 52 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1510-371T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541144 | ||||||
chr16:20541172
|
T | G | 213 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(210): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1510-399A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541172 | ||||||
chr16:20541221
|
G | A | 1 | a0004c0005t0006g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510-448C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541221 | ||||||
chr16:20541240
|
A | C | 25 | a0001c0002t0003g0012a0001c0002t0003g0112a0001c0002t0003g0262others(22): Show | 26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-467T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541240 | ||||||
chr16:20541244
|
T | A | 25 | a0001c0002t0003g0012a0001c0002t0003g0112a0001c0002t0003g0262others(22): Show | 26 | HG01081.hp2 HG01099.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1510-471A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541244 | ||||||
chr16:20541314
|
G | T | 41 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(38): Show | 47 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1510-541C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541314 | ||||||
chr16:20541350
|
A | G | 3 | a0001c0002t0002g0237a0001c0002t0002g0238a0001c0002t0002g0315 | 3 | HG00558.hp2 HG00738.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1510-577T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541350 | ||||||
chr16:20541444
|
G | A | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1510-671C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541444 | ||||||
chr16:20541470
|
C | A | 16 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(13): Show | 17 | HG01934.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1510-697G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541470 | ||||||
chr16:20541475
|
T | C | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-702A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541475 | ||||||
chr16:20541479
|
C | T | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-706G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541479 | ||||||
chr16:20541526
|
G | T | 1 | a0001c0002t0007g0294 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1510-753C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541526 | ||||||
chr16:20541546
|
C | G | 5 | a0001c0006t0011g0110a0003c0008t0011g0316a0003c0008t0011g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-773G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541546 | ||||||
chr16:20541560
|
T | C | 1 | a0001c0002t0004g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1510-787A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541560 | ||||||
chr16:20541572
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1510-799T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541572 | ||||||
chr16:20541674
|
T | A | 1 | a0003c0025t0003g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1510-901A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541674 | ||||||
chr16:20541674
|
T | C | 5 | a0003c0008t0003g0122a0005c0011t0026g0327a0006c0020t0003g0105others(2): Show | 5 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-901A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541674 | ||||||
chr16:20541675
|
T | C | 1 | a0001c0002t0002g0242 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-902A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541675 | ||||||
chr16:20541676
|
TC | T | 6 | a0003c0008t0003g0122a0003c0025t0003g0121a0005c0011t0026g0327others(3): Show | 6 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-904delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541676 | ||||||
chr16:20541677
|
C | T | 1 | a0001c0002t0002g0242 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-904G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541677 | ||||||
chr16:20541678
|
T | C | 1 | a0001c0012t0007g0024 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1510-905A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541678 | ||||||
chr16:20541679
|
T | C | 1 | a0001c0002t0002g0242 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510-906A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541679 | ||||||
chr16:20541679
|
TTC | T | 92 | a0001c0002t0002g0235a0001c0002t0003g0012a0001c0002t0003g0029others(89): Show | 101 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.1510-908_1510-907d others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541679 | ||||||
chr16:20541680
|
TC | T | 110 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(107): Show | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1510-908delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541680 | ||||||
chr16:20541681
|
C | T | 11 | a0001c0002t0002g0237a0001c0002t0002g0242a0001c0002t0002g0291others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1510-908G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541681 | ||||||
chr16:20541681
|
CT | C | 35 | a0001c0001t0001g0163a0001c0001t0003g0006a0001c0001t0003g0014others(32): Show | 41 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1510-909delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541681 | ||||||
chr16:20541684
|
T | C | 1 | a0001c0004t0002g0189 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1510-911A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541684 | ||||||
chr16:20541684
|
T | TC | 5 | a0003c0008t0003g0122a0005c0011t0026g0327a0006c0020t0003g0105others(2): Show | 5 | HG02630.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-912_1510-911i others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541684 | ||||||
chr16:20541685
|
T | C | 3 | a0001c0001t0001g0216a0001c0002t0003g0262a0003c0025t0003g0121 | 3 | HG01081.hp2 HG03704.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1510-912A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541685 | ||||||
chr16:20541713
|
C | T | 261 | a0001c0001t0001g0019a0001c0001t0001g0198a0001c0001t0003g0006others(258): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.1510-940G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541713 | ||||||
chr16:20541717
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0204 | 2 | NA19002.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1510-944G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541717 | ||||||
chr16:20541740
|
A | G | 7 | a0001c0001t0001g0207a0001c0002t0002g0242a0001c0002t0002g0288others(4): Show | 7 | HG01496.hp2 HG02015.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-967T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541740 | ||||||
chr16:20541744
|
G | A | 7 | a0001c0001t0001g0207a0001c0002t0002g0242a0001c0002t0002g0288others(4): Show | 7 | HG01168.hp2 HG01496.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-971C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541744 | ||||||
chr16:20541745
|
C | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1510-972G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541745 | ||||||
chr16:20541764
|
A | C | 218 | a0001c0001t0001g0201a0001c0002t0002g0007a0001c0002t0002g0025others(215): Show | 237 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1510-991T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541764 | ||||||
chr16:20541838
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0192a0001c0001t0001g0195others(3): Show | 6 | HG03209.hp1 NA18942.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-1065C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541838 | ||||||
chr16:20541884
|
T | C | 1 | a0004c0005t0006g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1509+1030A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541884 | ||||||
chr16:20541933
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0212others(1): Show | 6 | HG02080.hp1 HG02717.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+981T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541933 | ||||||
chr16:20541959
|
C | A | 3 | a0003c0008t0003g0122a0003c0025t0003g0121a0010c0023t0027g0332 | 3 | HG02630.hp2 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1509+955G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20541959 | ||||||
chr16:20542006
|
C | A | 146 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0111others(143): Show | 160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1509+908G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542006 | ||||||
chr16:20542026
|
G | A | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1509+888C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542026 | ||||||
chr16:20542150
|
G | A | 9 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+764C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542150 | ||||||
chr16:20542161
|
T | C | 121 | a0001c0001t0001g0019a0001c0001t0001g0170a0001c0001t0001g0201others(118): Show | 137 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.1509+753A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542161 | ||||||
chr16:20542175
|
T | G | 7 | a0001c0002t0002g0236a0003c0007t0014g0340a0003c0007t0014g0341others(4): Show | 7 | HG01109.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+739A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542175 | ||||||
chr16:20542193
|
C | T | 4 | a0001c0006t0011g0110a0003c0007t0014g0342a0003c0007t0014g0343others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+721G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542193 | ||||||
chr16:20542201
|
T | TTCTA | 19 | a0001c0002t0002g0242a0001c0002t0003g0012a0001c0006t0011g0110others(16): Show | 20 | HG01496.hp2 HG01934.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+712_1509+713i others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542201 | ||||||
chr16:20542202
|
G | T | 20 | a0001c0002t0002g0242a0001c0002t0003g0012a0001c0006t0011g0110others(17): Show | 21 | HG01496.hp2 HG01934.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1509+712C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542202 | ||||||
chr16:20542214
|
C | T | 30 | a0001c0002t0002g0291a0001c0002t0003g0260a0001c0002t0003g0263others(27): Show | 31 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1509+700G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542214 | ||||||
chr16:20542217
|
C | A | 30 | a0001c0002t0002g0291a0001c0002t0003g0260a0001c0002t0003g0263others(27): Show | 31 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1509+697G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542217 | ||||||
chr16:20542255
|
C | T | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1509+659G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542255 | ||||||
chr16:20542286
|
T | C | 3 | a0008c0013t0002g0108a0008c0013t0002g0109a0010c0023t0027g0332 | 3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1509+628A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542286 | ||||||
chr16:20542317
|
G | A | 143 | a0001c0001t0001g0201a0001c0001t0003g0177a0001c0001t0003g0184others(140): Show | 159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1509+597C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542317 | ||||||
chr16:20542328
|
T | A | 194 | a0001c0001t0001g0201a0001c0001t0001g0214a0001c0001t0003g0177others(191): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1509+586A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542328 | ||||||
chr16:20542335
|
T | C | 211 | a0001c0001t0001g0201a0001c0001t0001g0214a0001c0001t0003g0177others(208): Show | 232 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1509+579A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542335 | ||||||
chr16:20542345
|
AAC | A | 5 | a0003c0007t0014g0340a0003c0007t0014g0341a0003c0007t0014g0342others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+567_1509+568d others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542345 | ||||||
chr16:20542369
|
C | T | 1 | a0001c0006t0011g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1509+545G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542369 | ||||||
chr16:20542383
|
G | C | 133 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160others(130): Show | 147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1509+531C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542383 | ||||||
chr16:20542389
|
A | G | 1 | a0001c0002t0004g0301 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1509+525T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542389 | ||||||
chr16:20542428
|
A | G | 1 | a0005c0011t0008g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1509+486T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542428 | ||||||
chr16:20542437
|
C | T | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1509+477G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542437 | ||||||
chr16:20542450
|
C | A | 1 | a0003c0007t0014g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509+464G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542450 | ||||||
chr16:20542504
|
T | C | 14 | a0001c0001t0001g0165a0001c0001t0003g0184a0003c0007t0007g0281others(11): Show | 15 | HG00438.hp1 HG02040.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1509+410A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542504 | ||||||
chr16:20542533
|
G | A | 101 | a0001c0001t0003g0177a0001c0002t0002g0007a0001c0002t0002g0025others(98): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1509+381C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542533 | ||||||
chr16:20542557
|
A | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0157a0001c0001t0003g0184others(1): Show | 6 | HG00438.hp1 HG00609.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+357T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542557 | ||||||
chr16:20542568
|
T | C | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1509+346A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542568 | ||||||
chr16:20542569
|
A | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0157a0001c0001t0003g0184others(1): Show | 6 | HG00438.hp1 HG00609.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+345T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542569 | ||||||
chr16:20542578
|
T | C | 1 | a0004c0005t0006g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1509+336A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542578 | ||||||
chr16:20542585
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(174): Show | 203 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1509+329A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542585 | ||||||
chr16:20542661
|
G | T | 1 | a0001c0006t0003g0313 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1509+253C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542661 | ||||||
chr16:20542683
|
C | T | 5 | a0003c0008t0001g0319a0003c0008t0011g0320a0003c0008t0011g0321others(2): Show | 6 | HG02145.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+231G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542683 | ||||||
chr16:20542737
|
A | G | 3 | a0001c0002t0003g0029a0001c0027t0003g0282a0002c0018t0005g0071 | 4 | HG02109.hp2 HG02818.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+177T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542737 | ||||||
chr16:20542738
|
A | G | 3 | a0001c0002t0003g0029a0001c0027t0003g0282a0002c0018t0005g0071 | 4 | HG02109.hp2 HG02818.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+176T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542738 | ||||||
chr16:20542759
|
C | T | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+155G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542759 | ||||||
chr16:20542770
|
A | G | 1 | a0002c0018t0005g0071 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1509+144T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542770 | ||||||
chr16:20542812
|
G | A | 1 | a0001c0004t0002g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1509+102C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542812 | ||||||
chr16:20542881
|
C | G | 9 | a0001c0002t0002g0237a0001c0002t0002g0238a0001c0002t0004g0290others(6): Show | 9 | HG00738.hp2 HG01261.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+33G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 12/13 | chr16 | 20542881 | ||||||
chr16:20543051
|
C | T | 1 | a0003c0033t0003g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1410-38G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/13 | chr16 | 20543051 | ||||||
chr16:20543070
|
G | A | 15 | a0001c0001t0001g0160a0003c0033t0003g0174a0006c0010t0003g0011others(12): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1410-57C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 11/13 | chr16 | 20543070 | ||||||
chr16:20543291
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 131 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1282-29C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543291 | ||||||
chr16:20543438
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-176A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543438 | ||||||
chr16:20543689
|
C | T | 1 | a0010c0023t0027g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1282-427G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543689 | ||||||
chr16:20543735
|
C | G | 32 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(29): Show | 32 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1282-473G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543735 | ||||||
chr16:20543752
|
A | G | 1 | a0011c0021t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1282-490T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543752 | ||||||
chr16:20543765
|
T | C | 9 | a0002c0003t0005g0056a0003c0007t0007g0281a0003c0007t0014g0340others(6): Show | 9 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-503A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543765 | ||||||
chr16:20543782
|
C | G | 8 | a0003c0007t0007g0281a0003c0007t0014g0340a0003c0007t0014g0341others(5): Show | 8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-520G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543782 | ||||||
chr16:20543818
|
A | T | 24 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(21): Show | 24 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1282-556T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543818 | ||||||
chr16:20543882
|
A | G | 8 | a0003c0007t0007g0281a0003c0007t0014g0340a0003c0007t0014g0341others(5): Show | 8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-620T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543882 | ||||||
chr16:20543937
|
T | A | 63 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(60): Show | 68 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(65): Show |
intron_variant | MODIFIER | c.1282-675A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20543937 | ||||||
chr16:20544071
|
G | T | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-809C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544071 | ||||||
chr16:20544098
|
A | G | 3 | a0001c0001t0001g0017a0002c0019t0006g0067a0002c0019t0006g0070 | 4 | NA18988.hp1 NA18989.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-836T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544098 | ||||||
chr16:20544116
|
C | T | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1282-854G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544116 | ||||||
chr16:20544152
|
T | C | 50 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(47): Show | 54 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.1282-890A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544152 | ||||||
chr16:20544268
|
C | A | 40 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(37): Show | 41 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.1281+889G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544268 | ||||||
chr16:20544380
|
C | G | 2 | a0003c0008t0011g0316a0003c0008t0011g0317 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1281+777G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544380 | ||||||
chr16:20544387
|
T | A | 32 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(29): Show | 33 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.1281+770A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544387 | ||||||
chr16:20544434
|
G | T | 50 | a0001c0002t0004g0265a0002c0003t0005g0009a0002c0003t0005g0041others(47): Show | 54 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.1281+723C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544434 | ||||||
chr16:20544560
|
G | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+597C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544560 | ||||||
chr16:20544579
|
A | G | 4 | a0008c0013t0002g0106a0008c0013t0002g0107a0008c0013t0002g0108others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+578T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544579 | ||||||
chr16:20544597
|
T | G | 1 | a0004c0005t0006g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1281+560A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544597 | ||||||
chr16:20544655
|
T | C | 3 | a0003c0008t0003g0122a0003c0025t0003g0121a0016c0028t0003g0118 | 3 | HG03098.hp1 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1281+502A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544655 | ||||||
chr16:20544761
|
C | T | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+396G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544761 | ||||||
chr16:20544763
|
A | C | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+394T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544763 | ||||||
chr16:20544764
|
C | T | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+393G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544764 | ||||||
chr16:20544804
|
T | G | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+353A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544804 | ||||||
chr16:20544982
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1281+175G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20544982 | ||||||
chr16:20545010
|
T | G | 1 | a0001c0006t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1281+147A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545010 | ||||||
chr16:20545041
|
C | G | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+116G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545041 | ||||||
chr16:20545054
|
T | C | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+103A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545054 | ||||||
chr16:20545055
|
A | G | 1 | a0001c0001t0001g0005 | 3 | NA18948.hp2 NA18964.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1281+102T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545055 | ||||||
chr16:20545060
|
A | G | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1281+97T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545060 | ||||||
chr16:20545101
|
C | T | 8 | a0003c0007t0007g0322a0003c0008t0001g0319a0003c0008t0011g0316others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+56G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 10/13 | chr16 | 20545101 | ||||||
chr16:20545378
|
G | A | 1 | a0002c0018t0005g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1180-120C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545378 | ||||||
chr16:20545383
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1180-125G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545383 | ||||||
chr16:20545431
|
C | G | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1180-173G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545431 | ||||||
chr16:20545528
|
C | T | 1 | a0001c0002t0004g0267 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1180-270G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545528 | ||||||
chr16:20545582
|
C | G | 8 | a0003c0007t0007g0281a0003c0007t0014g0340a0003c0007t0014g0341others(5): Show | 8 | HG02258.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-324G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545582 | ||||||
chr16:20545612
|
AG | A | 3 | a0001c0001t0001g0134a0001c0004t0002g0137a0001c0004t0002g0141 | 3 | HG02602.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1180-355delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545612 | ||||||
chr16:20545699
|
T | C | 2 | a0001c0002t0007g0104a0005c0024t0016g0334 | 2 | HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1180-441A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545699 | ||||||
chr16:20545705
|
T | A | 11 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(8): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-447A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545705 | ||||||
chr16:20545714
|
A | T | 23 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(20): Show | 23 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1180-456T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545714 | ||||||
chr16:20545756
|
G | T | 1 | a0001c0006t0001g0306 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1180-498C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545756 | ||||||
chr16:20545789
|
C | A | 8 | a0003c0007t0007g0322a0003c0008t0001g0319a0003c0008t0011g0316others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-531G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545789 | ||||||
chr16:20545911
|
T | C | 2 | a0005c0011t0026g0327a0005c0016t0016g0326 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1179+483A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545911 | ||||||
chr16:20545940
|
C | T | 1 | a0005c0016t0029g0324 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1179+454G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545940 | ||||||
chr16:20545955
|
C | T | 8 | a0003c0007t0007g0322a0003c0008t0001g0319a0003c0008t0011g0316others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+439G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545955 | ||||||
chr16:20545985
|
T | A | 24 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(21): Show | 24 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1179+409A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20545985 | ||||||
chr16:20546053
|
G | C | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1179+341C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546053 | ||||||
chr16:20546211
|
T | C | 32 | a0003c0007t0003g0119a0003c0007t0003g0120a0003c0007t0003g0240others(29): Show | 33 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.1179+183A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546211 | ||||||
chr16:20546298
|
T | G | 63 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(60): Show | 68 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(65): Show |
intron_variant | MODIFIER | c.1179+96A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546298 | ||||||
chr16:20546312
|
A | T | 49 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(46): Show | 53 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.1179+82T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546312 | ||||||
chr16:20546339
|
T | C | 8 | a0003c0007t0007g0322a0003c0008t0001g0319a0003c0008t0011g0316others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+55A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546339 | ||||||
chr16:20546362
|
A | T | 2 | a0002c0003t0005g0081a0003c0008t0015g0318 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+32T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546362 | ||||||
chr16:20546366
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(114): Show | 139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1179+28A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 9/13 | chr16 | 20546366 | ||||||
chr16:20546511
|
A | G | 1 | a0001c0006t0003g0314 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1099-37T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546511 | ||||||
chr16:20546553
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1099-79G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546553 | ||||||
chr16:20546613
|
C | T | 21 | a0003c0007t0003g0119a0003c0007t0003g0120a0004c0005t0006g0040others(18): Show | 21 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099-139G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546613 | ||||||
chr16:20546638
|
T | C | 6 | a0001c0004t0002g0127a0002c0003t0005g0050a0003c0008t0011g0316others(3): Show | 6 | HG01256.hp2 HG02257.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-164A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546638 | ||||||
chr16:20546652
|
G | T | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1099-178C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546652 | ||||||
chr16:20546654
|
C | T | 4 | a0001c0002t0002g0315a0001c0004t0002g0127a0003c0008t0011g0316others(1): Show | 4 | HG00558.hp2 HG01256.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-180G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546654 | ||||||
chr16:20546657
|
A | G | 4 | a0001c0002t0002g0315a0001c0004t0002g0127a0003c0008t0011g0316others(1): Show | 4 | HG00558.hp2 HG01256.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-183T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546657 | ||||||
chr16:20546668
|
T | A | 51 | a0001c0006t0001g0293a0002c0003t0005g0009a0002c0003t0005g0041others(48): Show | 55 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(52): Show |
intron_variant | MODIFIER | c.1099-194A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546668 | ||||||
chr16:20546743
|
G | A | 4 | a0001c0002t0002g0242a0001c0002t0004g0285a0001c0006t0001g0289others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-269C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546743 | ||||||
chr16:20546744
|
T | C | 4 | a0001c0002t0002g0242a0001c0002t0004g0285a0001c0006t0001g0289others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-270A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546744 | ||||||
chr16:20546761
|
G | A | 3 | a0001c0002t0004g0285a0001c0006t0001g0289a0001c0006t0001g0296 | 3 | HG00733.hp1 HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1099-287C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546761 | ||||||
chr16:20546763
|
T | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-289A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546763 | ||||||
chr16:20546783
|
G | T | 3 | a0001c0002t0004g0285a0001c0006t0001g0289a0001c0006t0001g0296 | 3 | HG00733.hp1 HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1099-309C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546783 | ||||||
chr16:20546825
|
A | C | 1 | a0004c0005t0006g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1099-351T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546825 | ||||||
chr16:20546879
|
G | A | 2 | a0001c0017t0004g0026a0001c0017t0004g0268 | 3 | HG02698.hp2 HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1099-405C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546879 | ||||||
chr16:20546907
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): Show | 134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1099-433C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546907 | ||||||
chr16:20546912
|
A | G | 2 | a0003c0007t0003g0119a0003c0007t0003g0120 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1099-438T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546912 | ||||||
chr16:20546978
|
G | A | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1099-504C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546978 | ||||||
chr16:20546991
|
C | T | 1 | a0003c0033t0003g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1099-517G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20546991 | ||||||
chr16:20547013
|
C | T | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-539G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547013 | ||||||
chr16:20547032
|
C | A | 4 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(1): Show | 4 | HG02717.hp1 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-558G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547032 | ||||||
chr16:20547042
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1099-568C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547042 | ||||||
chr16:20547119
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 150 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1099-645T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547119 | ||||||
chr16:20547187
|
G | A | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-713C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547187 | ||||||
chr16:20547238
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099-764A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547238 | ||||||
chr16:20547246
|
T | C | 1 | a0001c0001t0003g0177 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099-772A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547246 | ||||||
chr16:20547277
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1098+785G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547277 | ||||||
chr16:20547445
|
T | G | 3 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1098+617A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547445 | ||||||
chr16:20547535
|
A | G | 3 | a0004c0005t0006g0094a0004c0005t0006g0096a0004c0005t0006g0100 | 3 | HG01934.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1098+527T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547535 | ||||||
chr16:20547612
|
C | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1098+450G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547612 | ||||||
chr16:20547742
|
G | C | 18 | a0001c0001t0003g0006a0001c0001t0003g0157a0001c0001t0003g0177others(15): Show | 21 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+320C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547742 | ||||||
chr16:20547767
|
C | G | 1 | a0007c0014t0001g0166 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1098+295G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547767 | ||||||
chr16:20547941
|
G | C | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+121C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20547941 | ||||||
chr16:20548017
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1098+45C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548017 | ||||||
chr16:20548022
|
A | G | 2 | a0001c0001t0001g0023a0001c0004t0007g0217 | 3 | NA18943.hp1 NA19002.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1098+40T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548022 | ||||||
chr16:20548032
|
A | C | 1 | a0001c0002t0002g0288 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+30T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 8/13 | chr16 | 20548032 | ||||||
chr16:20548243
|
G | C | 1 | a0002c0003t0005g0066 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.975-58C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548243 | ||||||
chr16:20548244
|
C | A | 1 | a0001c0001t0003g0132 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.975-59G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548244 | ||||||
chr16:20548252
|
T | G | 8 | a0001c0001t0001g0191a0001c0001t0003g0132a0001c0002t0003g0012others(5): Show | 9 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.975-67A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548252 | ||||||
chr16:20548307
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+87C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548307 | ||||||
chr16:20548349
|
G | A | 5 | a0004c0005t0006g0092a0004c0005t0006g0093a0004c0005t0006g0097others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+45C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 7/13 | chr16 | 20548349 | ||||||
chr16:20548548
|
A | G | 1 | a0003c0025t0003g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.895-75T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548548 | ||||||
chr16:20548715
|
T | C | 26 | a0001c0002t0003g0262a0001c0002t0004g0003a0001c0002t0004g0027others(23): Show | 32 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.895-242A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548715 | ||||||
chr16:20548722
|
C | A | 1 | a0001c0002t0004g0301 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.895-249G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548722 | ||||||
chr16:20548765
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(82): Show | 105 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.895-292T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548765 | ||||||
chr16:20548781
|
G | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-308C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548781 | ||||||
chr16:20548786
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(121): Show | 148 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.895-313A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548786 | ||||||
chr16:20548803
|
C | T | 13 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(10): Show | 14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.895-330G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548803 | ||||||
chr16:20548885
|
T | A | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.895-412A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548885 | ||||||
chr16:20548986
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.895-513T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20548986 | ||||||
chr16:20549055
|
T | C | 86 | a0001c0002t0003g0012a0002c0003t0005g0009a0002c0003t0005g0041others(83): Show | 92 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(89): Show |
intron_variant | MODIFIER | c.895-582A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549055 | ||||||
chr16:20549091
|
A | G | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-618T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549091 | ||||||
chr16:20549286
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.895-813A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549286 | ||||||
chr16:20549402
|
T | G | 1 | a0001c0012t0007g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.895-929A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549402 | ||||||
chr16:20549427
|
C | T | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-954G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549427 | ||||||
chr16:20549431
|
T | C | 3 | a0002c0003t0013g0047a0002c0003t0013g0048a0002c0003t0013g0049 | 3 | HG02145.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.895-958A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549431 | ||||||
chr16:20549691
|
G | A | 3 | a0001c0001t0012g0008a0001c0001t0012g0035a0001c0001t0012g0036 | 4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-1218C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549691 | ||||||
chr16:20549712
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.895-1239G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549712 | ||||||
chr16:20549764
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.895-1291A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549764 | ||||||
chr16:20549771
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.895-1298A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549771 | ||||||
chr16:20549824
|
TA | T | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1352delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549824 | ||||||
chr16:20549836
|
T | G | 1 | a0001c0001t0003g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.895-1363A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549836 | ||||||
chr16:20549868
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 240 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.895-1395C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549868 | ||||||
chr16:20549998
|
A | AT | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(121): Show | 148 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.895-1526dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20549998 | ||||||
chr16:20550007
|
T | A | 37 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(34): Show | 39 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.895-1534A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550007 | ||||||
chr16:20550166
|
C | A | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.895-1693G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550166 | ||||||
chr16:20550268
|
A | G | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.895-1795T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550268 | ||||||
chr16:20550284
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(80): Show | 103 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.895-1811A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550284 | ||||||
chr16:20550295
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.895-1822G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550295 | ||||||
chr16:20550451
|
T | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.894+1693A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550451 | ||||||
chr16:20550474
|
G | T | 1 | a0001c0002t0004g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.894+1670C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550474 | ||||||
chr16:20550500
|
T | G | 13 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(10): Show | 14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+1644A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550500 | ||||||
chr16:20550561
|
C | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.894+1583G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550561 | ||||||
chr16:20550625
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.894+1519C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550625 | ||||||
chr16:20550664
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.894+1480C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550664 | ||||||
chr16:20550689
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.894+1455C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550689 | ||||||
chr16:20550756
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.894+1388G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550756 | ||||||
chr16:20550820
|
A | G | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.894+1324T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550820 | ||||||
chr16:20550842
|
G | C | 1 | a0001c0002t0004g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+1302C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20550842 | ||||||
chr16:20551055
|
A | G | 2 | a0001c0002t0004g0311a0001c0002t0004g0312 | 2 | HG02083.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.894+1089T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551055 | ||||||
chr16:20551165
|
A | G | 1 | a0001c0002t0003g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.894+979T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551165 | ||||||
chr16:20551166
|
C | T | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+978G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551166 | ||||||
chr16:20551267
|
G | T | 4 | a0002c0003t0005g0081a0002c0003t0005g0082a0002c0003t0005g0084others(1): Show | 4 | HG02559.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+877C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551267 | ||||||
chr16:20551276
|
G | C | 1 | a0001c0001t0001g0001 | 6 | NA18970.hp1 NA18972.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.894+868C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551276 | ||||||
chr16:20551337
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(201): Show | 233 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.894+807A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551337 | ||||||
chr16:20551353
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(219): Show | 253 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.894+791A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551353 | ||||||
chr16:20551409
|
T | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(200): Show | 232 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.894+735A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551409 | ||||||
chr16:20551415
|
T | C | 106 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(103): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.894+729A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551415 | ||||||
chr16:20551424
|
T | G | 105 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(102): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.894+720A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551424 | ||||||
chr16:20551529
|
T | C | 1 | a0001c0001t0003g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.894+615A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551529 | ||||||
chr16:20551532
|
T | C | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+612A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551532 | ||||||
chr16:20551768
|
AAC | A | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+374_894+375del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551768 | ||||||
chr16:20551793
|
G | A | 2 | a0011c0021t0001g0193a0011c0021t0001g0194 | 2 | HG03831.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.894+351C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551793 | ||||||
chr16:20551799
|
G | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0195a0001c0001t0001g0197others(2): Show | 5 | NA18942.hp2 NA19063.hp1 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+345C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551799 | ||||||
chr16:20551837
|
G | A | 13 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(10): Show | 14 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+307C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551837 | ||||||
chr16:20551871
|
T | C | 4 | a0003c0007t0014g0340a0003c0007t0014g0341a0003c0007t0014g0342others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+273A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551871 | ||||||
chr16:20551878
|
G | C | 4 | a0008c0013t0002g0106a0008c0013t0002g0107a0008c0013t0002g0108others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+266C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551878 | ||||||
chr16:20551931
|
A | G | 80 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(77): Show | 85 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(82): Show |
intron_variant | MODIFIER | c.894+213T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551931 | ||||||
chr16:20551946
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(81): Show | 104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.894+198T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551946 | ||||||
chr16:20551958
|
G | C | 4 | a0001c0017t0004g0026a0002c0003t0013g0047a0002c0003t0013g0048others(1): Show | 5 | HG02145.hp1 HG02486.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+186C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551958 | ||||||
chr16:20551974
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.894+170G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20551974 | ||||||
chr16:20552010
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.894+134C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20552010 | ||||||
chr16:20552020
|
C | T | 1 | a0001c0002t0007g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.894+124G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 6/13 | chr16 | 20552020 | ||||||
chr16:20552341
|
G | A | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-44C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552341 | ||||||
chr16:20552351
|
C | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.741-54G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552351 | ||||||
chr16:20552364
|
G | C | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-67C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552364 | ||||||
chr16:20552404
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.741-107G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552404 | ||||||
chr16:20552405
|
G | A | 71 | a0001c0002t0007g0104a0002c0003t0005g0009a0002c0003t0005g0041others(68): Show | 75 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(72): Show |
intron_variant | MODIFIER | c.741-108C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552405 | ||||||
chr16:20552430
|
C | A | 80 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(77): Show | 85 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(82): Show |
intron_variant | MODIFIER | c.741-133G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552430 | ||||||
chr16:20552437
|
T | C | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-140A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552437 | ||||||
chr16:20552440
|
A | T | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-143T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552440 | ||||||
chr16:20552447
|
G | A | 1 | a0001c0002t0003g0012 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.741-150C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552447 | ||||||
chr16:20552457
|
G | A | 5 | a0001c0002t0004g0030a0001c0002t0004g0270a0001c0002t0004g0297others(2): Show | 6 | HG00438.hp2 NA18945.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.741-160C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552457 | ||||||
chr16:20552474
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-177C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552474 | ||||||
chr16:20552488
|
C | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.741-191G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552488 | ||||||
chr16:20552488
|
C | T | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-191G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552488 | ||||||
chr16:20552491
|
T | C | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-194A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552491 | ||||||
chr16:20552492
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-195C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552492 | ||||||
chr16:20552494
|
T | C | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-197A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552494 | ||||||
chr16:20552506
|
G | A | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.741-209C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552506 | ||||||
chr16:20552510
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-213C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552510 | ||||||
chr16:20552525
|
A | G | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-228T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552525 | ||||||
chr16:20552541
|
T | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.741-244A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552541 | ||||||
chr16:20552636
|
G | A | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.741-339C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552636 | ||||||
chr16:20552637
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(328): Show | 374 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.741-340T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552637 | ||||||
chr16:20552683
|
T | C | 3 | a0001c0002t0007g0104a0005c0024t0016g0334a0010c0022t0008g0325 | 3 | HG02630.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.741-386A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552683 | ||||||
chr16:20552851
|
C | T | 1 | a0001c0006t0003g0313 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.741-554G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552851 | ||||||
chr16:20552859
|
G | A | 1 | a0001c0002t0002g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.741-562C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552859 | ||||||
chr16:20552978
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.741-681G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552978 | ||||||
chr16:20552981
|
C | T | 4 | a0002c0003t0005g0044a0002c0003t0005g0046a0002c0003t0005g0051others(1): Show | 4 | NA18959.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-684G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20552981 | ||||||
chr16:20553065
|
A | G | 3 | a0005c0011t0008g0328a0005c0011t0008g0330a0005c0011t0008g0331 | 3 | HG01168.hp1 HG01169.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.740+712T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553065 | ||||||
chr16:20553068
|
G | T | 25 | a0001c0002t0003g0262a0001c0002t0004g0003a0001c0002t0004g0027others(22): Show | 31 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.740+709C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553068 | ||||||
chr16:20553118
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(80): Show | 103 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.740+659A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553118 | ||||||
chr16:20553171
|
T | C | 97 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(94): Show | 103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.740+606A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553171 | ||||||
chr16:20553347
|
G | A | 1 | a0001c0002t0004g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.740+430C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553347 | ||||||
chr16:20553407
|
A | G | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.740+370T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553407 | ||||||
chr16:20553420
|
A | C | 1 | a0001c0002t0004g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.740+357T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553420 | ||||||
chr16:20553523
|
A | G | 1 | a0001c0002t0003g0263 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.740+254T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553523 | ||||||
chr16:20553608
|
G | T | 1 | a0002c0003t0010g0053 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.740+169C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553608 | ||||||
chr16:20553617
|
T | C | 2 | a0005c0011t0026g0327a0005c0016t0016g0326 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.740+160A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553617 | ||||||
chr16:20553681
|
A | G | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.740+96T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553681 | ||||||
chr16:20553698
|
A | G | 1 | a0001c0004t0002g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.740+79T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553698 | ||||||
chr16:20553753
|
G | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0172a0001c0001t0001g0218others(1): Show | 5 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.740+24C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 5/13 | chr16 | 20553753 | ||||||
chr16:20554002
|
A | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.597-82T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554002 | ||||||
chr16:20554017
|
G | A | 1 | a0001c0002t0002g0242 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.597-97C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554017 | ||||||
chr16:20554072
|
A | C | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.597-152T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554072 | ||||||
chr16:20554074
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.597-154G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554074 | ||||||
chr16:20554263
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.597-343C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554263 | ||||||
chr16:20554298
|
C | T | 1 | a0007c0014t0001g0200 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.597-378G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554298 | ||||||
chr16:20554344
|
T | A | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.597-424A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554344 | ||||||
chr16:20554406
|
A | T | 1 | a0001c0002t0002g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.597-486T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554406 | ||||||
chr16:20554416
|
T | C | 1 | a0001c0002t0004g0270 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.597-496A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554416 | ||||||
chr16:20554485
|
G | T | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-565C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554485 | ||||||
chr16:20554493
|
G | A | 36 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(33): Show | 40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.597-573C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554493 | ||||||
chr16:20554528
|
A | T | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.597-608T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554528 | ||||||
chr16:20554572
|
G | A | 1 | a0002c0003t0005g0041 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.597-652C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554572 | ||||||
chr16:20554736
|
G | C | 1 | a0008c0013t0002g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.596+533C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554736 | ||||||
chr16:20554776
|
T | G | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.596+493A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554776 | ||||||
chr16:20554895
|
T | C | 1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+374A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554895 | ||||||
chr16:20554911
|
C | G | 7 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(4): Show | 7 | HG01109.hp1 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.596+358G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554911 | ||||||
chr16:20554932
|
C | T | 1 | a0001c0004t0002g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.596+337G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554932 | ||||||
chr16:20554965
|
C | G | 97 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(94): Show | 103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+304G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20554965 | ||||||
chr16:20555010
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.596+259C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555010 | ||||||
chr16:20555024
|
T | TA | 3 | a0001c0001t0001g0134a0001c0004t0002g0137a0001c0004t0002g0141 | 3 | HG02602.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.596+244dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555024 | ||||||
chr16:20555107
|
G | GA | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 252 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.596+161dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555107 | ||||||
chr16:20555156
|
T | G | 1 | a0003c0025t0003g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.596+113A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555156 | ||||||
chr16:20555246
|
G | C | 8 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.596+23C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 4/13 | chr16 | 20555246 | ||||||
chr16:20555671
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.389-195C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555671 | ||||||
chr16:20555798
|
C | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.389-322G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555798 | ||||||
chr16:20555875
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.389-399T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555875 | ||||||
chr16:20555955
|
T | A | 2 | a0004c0005t0006g0099a0004c0005t0006g0103 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.389-479A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20555955 | ||||||
chr16:20556016
|
T | C | 106 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(103): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.389-540A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556016 | ||||||
chr16:20556088
|
AT | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.389-613delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556088 | ||||||
chr16:20556160
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-684C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556160 | ||||||
chr16:20556356
|
C | T | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.389-880G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556356 | ||||||
chr16:20556381
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.389-905A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556381 | ||||||
chr16:20556422
|
C | T | 1 | a0001c0004t0004g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.389-946G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556422 | ||||||
chr16:20556444
|
A | G | 1 | a0004c0005t0006g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389-968T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556444 | ||||||
chr16:20556466
|
G | T | 1 | a0001c0002t0007g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.389-990C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556466 | ||||||
chr16:20556524
|
C | T | 1 | a0001c0004t0004g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.389-1048G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556524 | ||||||
chr16:20556567
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1091T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556567 | ||||||
chr16:20556721
|
T | C | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.389-1245A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556721 | ||||||
chr16:20556780
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1304T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556780 | ||||||
chr16:20556938
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1462T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20556938 | ||||||
chr16:20557017
|
G | A | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-1541C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557017 | ||||||
chr16:20557180
|
C | G | 1 | a0001c0002t0004g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.389-1704G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557180 | ||||||
chr16:20557194
|
C | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(126): Show | 153 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.389-1718G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557194 | ||||||
chr16:20557199
|
A | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.389-1723T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557199 | ||||||
chr16:20557216
|
CT | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.389-1741delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557216 | ||||||
chr16:20557240
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.389-1764G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557240 | ||||||
chr16:20557268
|
G | C | 1 | a0003c0007t0014g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.389-1792C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557268 | ||||||
chr16:20557271
|
A | C | 1 | a0007c0014t0001g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.389-1795T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557271 | ||||||
chr16:20557290
|
A | G | 1 | a0001c0002t0002g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.389-1814T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557290 | ||||||
chr16:20557404
|
T | G | 1 | a0001c0002t0004g0304 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.388+1833A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557404 | ||||||
chr16:20557405
|
TC | T | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.388+1831delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557405 | ||||||
chr16:20557408
|
C | A | 47 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(44): Show | 49 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.388+1829G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557408 | ||||||
chr16:20557434
|
ATCTCCAT others(1): Show |
A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1795_388+1802d others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557434 | ||||||
chr16:20557443
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1794A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557443 | ||||||
chr16:20557486
|
T | C | 1 | a0001c0001t0008g0336 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.388+1751A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557486 | ||||||
chr16:20557521
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.388+1716G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557521 | ||||||
chr16:20557546
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(81): Show | 104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.388+1691G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557546 | ||||||
chr16:20557686
|
T | A | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+1551A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557686 | ||||||
chr16:20557713
|
C | T | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+1524G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557713 | ||||||
chr16:20557783
|
T | A | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1454A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557783 | ||||||
chr16:20557800
|
T | C | 1 | a0001c0002t0004g0277 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.388+1437A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557800 | ||||||
chr16:20557803
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1434G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557803 | ||||||
chr16:20557821
|
C | G | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+1416G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557821 | ||||||
chr16:20557833
|
T | A | 1 | a0004c0005t0006g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.388+1404A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557833 | ||||||
chr16:20557972
|
A | T | 1 | a0001c0004t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.388+1265T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20557972 | ||||||
chr16:20558059
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.388+1178G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558059 | ||||||
chr16:20558124
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+1113G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558124 | ||||||
chr16:20558125
|
G | A | 1 | a0002c0003t0005g0072 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.388+1112C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558125 | ||||||
chr16:20558233
|
A | G | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.388+1004T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558233 | ||||||
chr16:20558335
|
C | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+902G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558335 | ||||||
chr16:20558336
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0211 | 3 | NA18945.hp2 NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.388+901G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558336 | ||||||
chr16:20558343
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(125): Show | 152 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.388+894G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558343 | ||||||
chr16:20558351
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+886G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558351 | ||||||
chr16:20558352
|
T | A | 1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388+885A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558352 | ||||||
chr16:20558354
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+883G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558354 | ||||||
chr16:20558691
|
A | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+546T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558691 | ||||||
chr16:20558714
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388+523T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558714 | ||||||
chr16:20558743
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.388+494C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558743 | ||||||
chr16:20558794
|
T | C | 1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.388+443A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558794 | ||||||
chr16:20558896
|
T | A | 3 | a0001c0002t0003g0029a0001c0027t0003g0282a0003c0007t0007g0281 | 4 | HG02109.hp2 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+341A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558896 | ||||||
chr16:20558902
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.388+335T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20558902 | ||||||
chr16:20559045
|
T | C | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388+192A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559045 | ||||||
chr16:20559143
|
C | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.388+94G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559143 | ||||||
chr16:20559144
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(217): Show | 251 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(248): Show |
intron_variant | MODIFIER | c.388+93T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 3/13 | chr16 | 20559144 | ||||||
chr16:20559453
|
G | T | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.178-6C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559453 | ||||||
chr16:20559462
|
A | G | 3 | a0004c0005t0006g0096a0009c0015t0008g0032a0009c0015t0008g0329 | 4 | HG01934.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-15T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559462 | ||||||
chr16:20559473
|
T | C | 2 | a0009c0015t0008g0032a0009c0015t0008g0329 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-26A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559473 | ||||||
chr16:20559515
|
C | T | 3 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178-68G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559515 | ||||||
chr16:20559530
|
C | T | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-83G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559530 | ||||||
chr16:20559540
|
G | A | 1 | a0006c0010t0003g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178-93C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559540 | ||||||
chr16:20559574
|
A | T | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-127T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559574 | ||||||
chr16:20559580
|
A | G | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-133T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559580 | ||||||
chr16:20559584
|
T | C | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-137A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559584 | ||||||
chr16:20559592
|
C | T | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-145G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559592 | ||||||
chr16:20559600
|
G | C | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-153C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559600 | ||||||
chr16:20559625
|
A | G | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-178T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559625 | ||||||
chr16:20559639
|
T | C | 105 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(102): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.178-192A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559639 | ||||||
chr16:20559721
|
AT | A | 85 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(82): Show | 90 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(87): Show |
intron_variant | MODIFIER | c.178-275delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559721 | ||||||
chr16:20559742
|
G | A | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-295C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559742 | ||||||
chr16:20559743
|
T | A | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-296A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559743 | ||||||
chr16:20559783
|
T | TTTTA | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-340_178-337dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559783 | ||||||
chr16:20559796
|
A | G | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-349T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559796 | ||||||
chr16:20559805
|
T | C | 13 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(10): Show | 14 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-358A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559805 | ||||||
chr16:20559812
|
A | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-365T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559812 | ||||||
chr16:20559823
|
T | C | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-376A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559823 | ||||||
chr16:20559836
|
T | A | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-389A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559836 | ||||||
chr16:20559841
|
T | A | 1 | a0001c0002t0004g0273 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178-394A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559841 | ||||||
chr16:20559848
|
C | G | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-401G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559848 | ||||||
chr16:20559894
|
T | C | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-447A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559894 | ||||||
chr16:20559921
|
T | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 160 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.178-474A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559921 | ||||||
chr16:20559944
|
C | A | 14 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-497G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559944 | ||||||
chr16:20559950
|
TCACTTTA others(1819): Show |
T | 2 | a0009c0015t0008g0032a0009c0015t0008g0329 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2329_178-504de others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559950 | ||||||
chr16:20559973
|
T | G | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-526A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559973 | ||||||
chr16:20559986
|
C | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-539G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20559986 | ||||||
chr16:20560006
|
G | A | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-559C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560006 | ||||||
chr16:20560031
|
G | A | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-584C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560031 | ||||||
chr16:20560114
|
GA | G | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-668delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560114 | ||||||
chr16:20560129
|
C | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(81): Show | 104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.178-682G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560129 | ||||||
chr16:20560135
|
C | T | 18 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(15): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.178-688G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560135 | ||||||
chr16:20560150
|
C | T | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-703G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560150 | ||||||
chr16:20560165
|
T | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-718A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560165 | ||||||
chr16:20560181
|
A | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-734T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560181 | ||||||
chr16:20560213
|
T | G | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-766A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560213 | ||||||
chr16:20560319
|
A | G | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-872T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560319 | ||||||
chr16:20560479
|
T | G | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1032A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560479 | ||||||
chr16:20560572
|
T | C | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-1125A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560572 | ||||||
chr16:20560586
|
T | G | 1 | a0001c0002t0004g0278 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.178-1139A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560586 | ||||||
chr16:20560650
|
T | C | 6 | a0003c0008t0003g0122a0004c0005t0006g0045a0004c0005t0006g0086others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-1203A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560650 | ||||||
chr16:20560783
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.178-1336C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560783 | ||||||
chr16:20560848
|
G | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-1401C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560848 | ||||||
chr16:20560899
|
G | A | 1 | a0008c0013t0002g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-1452C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560899 | ||||||
chr16:20560924
|
A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-1477T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560924 | ||||||
chr16:20560927
|
A | G | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178-1480T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20560927 | ||||||
chr16:20561054
|
C | T | 2 | a0001c0004t0002g0128a0001c0004t0002g0133 | 2 | NA18966.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.178-1607G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561054 | ||||||
chr16:20561102
|
T | C | 97 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(94): Show | 103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.178-1655A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561102 | ||||||
chr16:20561143
|
C | G | 105 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(102): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.178-1696G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561143 | ||||||
chr16:20561170
|
C | A | 2 | a0005c0024t0016g0334a0010c0022t0008g0325 | 2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.178-1723G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561170 | ||||||
chr16:20561170
|
C | G | 1 | a0001c0006t0003g0314 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.178-1723G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561170 | ||||||
chr16:20561230
|
C | T | 1 | a0001c0001t0008g0335 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.178-1783G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561230 | ||||||
chr16:20561241
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.178-1794A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561241 | ||||||
chr16:20561369
|
C | T | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.178-1922G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561369 | ||||||
chr16:20561385
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-1938C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561385 | ||||||
chr16:20561387
|
G | T | 1 | a0001c0002t0007g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-1940C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561387 | ||||||
chr16:20561526
|
G | T | 19 | a0004c0005t0006g0040a0004c0005t0006g0045a0004c0005t0006g0086others(16): Show | 19 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-2079C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561526 | ||||||
chr16:20561528
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.178-2081G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561528 | ||||||
chr16:20561643
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178-2196G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561643 | ||||||
chr16:20561684
|
C | CT | 5 | a0001c0001t0003g0177a0001c0002t0003g0012a0003c0007t0003g0119others(2): Show | 6 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-2238dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561684 | ||||||
chr16:20561684
|
CT | C | 37 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(34): Show | 41 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.178-2238delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561684 | ||||||
chr16:20561811
|
C | A | 65 | a0001c0002t0002g0288a0001c0002t0002g0291a0001c0002t0002g0302others(62): Show | 73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.178-2364G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561811 | ||||||
chr16:20561821
|
A | G | 2 | a0009c0015t0008g0032a0009c0015t0008g0329 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2374T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561821 | ||||||
chr16:20561843
|
G | A | 3 | a0001c0001t0001g0156a0009c0015t0008g0032a0009c0015t0008g0329 | 4 | HG03490.hp2 HG03492.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-2396C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561843 | ||||||
chr16:20561860
|
C | A | 7 | a0001c0001t0001g0147a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 9 | HG00597.hp1 HG00621.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-2413G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561860 | ||||||
chr16:20561866
|
C | T | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-2419G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561866 | ||||||
chr16:20561905
|
T | C | 1 | a0013c0031t0016g0338 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.178-2458A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561905 | ||||||
chr16:20561949
|
T | A | 18 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(15): Show | 19 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178-2502A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561949 | ||||||
chr16:20561960
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.178-2513T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561960 | ||||||
chr16:20561968
|
G | GT | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(322): Show | 368 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(365): Show |
intron_variant | MODIFIER | c.178-2522dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561968 | ||||||
chr16:20561968
|
G | T | 1 | a0001c0006t0003g0313 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178-2521C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561968 | ||||||
chr16:20561979
|
C | CTTGCCAT others(3): Show |
2 | a0009c0015t0008g0032a0009c0015t0008g0329 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-2542_178-2533d others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20561979 | ||||||
chr16:20562090
|
T | A | 1 | a0001c0002t0003g0012 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.177+2579A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562090 | ||||||
chr16:20562095
|
A | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.177+2574T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562095 | ||||||
chr16:20562098
|
T | C | 1 | a0015c0032t0025g0339 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.177+2571A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562098 | ||||||
chr16:20562137
|
A | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+2532T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562137 | ||||||
chr16:20562138
|
C | A | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+2531G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562138 | ||||||
chr16:20562185
|
A | G | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2484T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562185 | ||||||
chr16:20562249
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.177+2420C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562249 | ||||||
chr16:20562253
|
C | T | 7 | a0006c0010t0003g0011a0006c0010t0003g0114a0006c0010t0003g0115others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+2416G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562253 | ||||||
chr16:20562325
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+2344A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562325 | ||||||
chr16:20562392
|
C | A | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2277G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562392 | ||||||
chr16:20562536
|
T | C | 14 | a0002c0003t0010g0004a0002c0018t0010g0039a0003c0007t0007g0322others(11): Show | 17 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+2133A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562536 | ||||||
chr16:20562548
|
A | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+2121T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562548 | ||||||
chr16:20562584
|
G | T | 1 | a0006c0010t0017g0037 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+2085C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562584 | ||||||
chr16:20562784
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.177+1885C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562784 | ||||||
chr16:20562866
|
C | A | 2 | a0001c0012t0007g0024a0001c0012t0007g0223 | 3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.177+1803G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562866 | ||||||
chr16:20562878
|
C | G | 1 | a0001c0002t0004g0323 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.177+1791G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562878 | ||||||
chr16:20562915
|
G | A | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+1754C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562915 | ||||||
chr16:20562960
|
C | A | 6 | a0001c0001t0001g0135a0001c0004t0002g0127a0001c0004t0002g0136others(3): Show | 6 | HG01074.hp1 HG01168.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1709G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20562960 | ||||||
chr16:20563063
|
C | G | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+1606G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563063 | ||||||
chr16:20563103
|
C | T | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.177+1566G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563103 | ||||||
chr16:20563143
|
A | G | 1 | a0005c0016t0029g0324 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+1526T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563143 | ||||||
chr16:20563144
|
A | T | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+1525T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563144 | ||||||
chr16:20563220
|
C | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.177+1449G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563220 | ||||||
chr16:20563429
|
A | G | 1 | a0001c0006t0003g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177+1240T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563429 | ||||||
chr16:20563587
|
A | T | 1 | a0001c0004t0002g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.177+1082T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563587 | ||||||
chr16:20563592
|
TA | T | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+1076delT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563592 | ||||||
chr16:20563680
|
G | T | 103 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(100): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.177+989C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563680 | ||||||
chr16:20563729
|
C | A | 105 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0222others(102): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.177+940G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563729 | ||||||
chr16:20563740
|
T | C | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+929A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563740 | ||||||
chr16:20563771
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.177+898C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563771 | ||||||
chr16:20563805
|
T | C | 4 | a0001c0002t0003g0260a0001c0002t0003g0261a0001c0002t0003g0263others(1): Show | 4 | HG02280.hp2 HG02451.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+864A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563805 | ||||||
chr16:20563985
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.177+684C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20563985 | ||||||
chr16:20564108
|
C | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+561G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564108 | ||||||
chr16:20564148
|
C | T | 4 | a0001c0001t0001g0123a0001c0004t0002g0126a0001c0004t0002g0129others(1): Show | 4 | NA18992.hp1 NA19001.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+521G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564148 | ||||||
chr16:20564151
|
T | A | 1 | a0001c0002t0007g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+518A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564151 | ||||||
chr16:20564274
|
A | G | 4 | a0001c0001t0001g0123a0001c0004t0002g0126a0001c0004t0002g0129others(1): Show | 4 | NA18992.hp1 NA19001.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+395T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564274 | ||||||
chr16:20564297
|
G | A | 2 | a0001c0012t0007g0024a0001c0012t0007g0223 | 3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.177+372C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564297 | ||||||
chr16:20564305
|
G | T | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.177+364C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564305 | ||||||
chr16:20564340
|
C | T | 11 | a0003c0007t0014g0340a0003c0007t0014g0341a0003c0007t0014g0342others(8): Show | 12 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+329G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564340 | ||||||
chr16:20564432
|
G | C | 1 | a0001c0002t0004g0273 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.177+237C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 2/13 | chr16 | 20564432 | ||||||
chr16:20564918
|
G | A | 1 | a0001c0002t0004g0323 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8-65C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564918 | ||||||
chr16:20564945
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-92A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564945 | ||||||
chr16:20564997
|
T | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-8-144A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20564997 | ||||||
chr16:20565039
|
G | T | 2 | a0005c0011t0019g0033a0005c0016t0028g0333 | 3 | HG01891.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-186C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565039 | ||||||
chr16:20565106
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-8-253G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565106 | ||||||
chr16:20565147
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-294C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565147 | ||||||
chr16:20565221
|
T | C | 2 | a0003c0008t0011g0316a0003c0008t0011g0317 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-368A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565221 | ||||||
chr16:20565231
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(234): Show | 270 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.-8-378T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565231 | ||||||
chr16:20565361
|
C | G | 3 | a0001c0001t0012g0008a0001c0001t0012g0035a0001c0001t0012g0036 | 4 | NA18953.hp1 NA18957.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-508G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565361 | ||||||
chr16:20565424
|
T | A | 47 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(44): Show | 49 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8-571A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565424 | ||||||
chr16:20565563
|
G | A | 3 | a0003c0008t0001g0319a0003c0008t0015g0031a0003c0008t0015g0318 | 4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-710C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565563 | ||||||
chr16:20565580
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-727A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565580 | ||||||
chr16:20565608
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-755C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565608 | ||||||
chr16:20565783
|
A | G | 1 | a0001c0002t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-930T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565783 | ||||||
chr16:20565954
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-1101C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565954 | ||||||
chr16:20565990
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-1137G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20565990 | ||||||
chr16:20566043
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 238 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.-8-1190A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566043 | ||||||
chr16:20566105
|
C | A | 2 | a0005c0011t0026g0327a0005c0016t0016g0326 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8-1252G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566105 | ||||||
chr16:20566105
|
C | T | 1 | a0006c0020t0003g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-1252G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566105 | ||||||
chr16:20566112
|
A | G | 1 | a0003c0025t0003g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-8-1259T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566112 | ||||||
chr16:20566115
|
T | TA | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(213): Show | 246 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.-8-1263dupT | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566115 | ||||||
chr16:20566130
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1277A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566130 | ||||||
chr16:20566131
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1278T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566131 | ||||||
chr16:20566173
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1320C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566173 | ||||||
chr16:20566212
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(234): Show | 270 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.-8-1359G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566212 | ||||||
chr16:20566247
|
T | TTA | 29 | a0001c0002t0002g0288a0001c0002t0002g0291a0001c0002t0004g0264others(26): Show | 30 | HG00323.hp2 HG00609.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8-1396_-8-1395dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTATA | 20 | a0001c0002t0002g0241a0001c0002t0002g0242a0001c0002t0002g0258others(17): Show | 23 | HG00280.hp1 HG01167.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1398_-8-1395dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTATATA | 21 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0247others(18): Show | 25 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-1400_-8-1395dup others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTATATAT others(1): Show |
3 | a0001c0002t0002g0259a0001c0002t0003g0260a0005c0011t0008g0331 | 3 | HG01169.hp1 HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1402_-8-1395dup others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTATATA others(6): Show |
1 | a0002c0018t0005g0071 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(13): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTTATA | 5 | a0002c0003t0005g0043a0002c0003t0005g0046a0002c0003t0005g0055others(2): Show | 5 | HG01891.hp2 HG01975.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTTATAT others(1): Show |
14 | a0002c0003t0005g0009a0002c0003t0005g0044a0002c0003t0005g0051others(11): Show | 15 | HG01257.hp1 HG02809.hp2 HG03195.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTTATAT others(3): Show |
15 | a0002c0003t0005g0042a0002c0003t0005g0052a0002c0003t0005g0064others(12): Show | 16 | HG00673.hp1 HG01943.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTTATAT others(5): Show |
7 | a0002c0003t0005g0050a0002c0003t0005g0068a0002c0003t0005g0069others(4): Show | 7 | HG01256.hp1 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
T | TTTTATAT others(7): Show |
2 | a0002c0003t0010g0053a0002c0003t0013g0049 | 2 | HG02486.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-8-1395_-8-1394ins others(14): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTA | T | 28 | a0001c0002t0002g0239a0001c0002t0002g0248a0001c0002t0002g0249others(25): Show | 29 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8-1396_-8-1395del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATA | T | 25 | a0001c0002t0002g0111a0001c0002t0002g0236a0001c0002t0002g0237others(22): Show | 26 | HG00738.hp2 HG01109.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-1398_-8-1395del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATA | T | 16 | a0001c0001t0001g0165a0001c0002t0002g0233a0001c0002t0002g0234others(13): Show | 18 | HG00558.hp2 HG00597.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-1400_-8-1395del others(6): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATAT others(1): Show |
T | 24 | a0001c0001t0001g0022a0001c0001t0001g0123a0001c0001t0001g0147others(21): Show | 30 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-1402_-8-1395del others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATAT others(3): Show |
T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 108 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-8-1404_-8-1395del others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATAT others(5): Show |
T | 5 | a0001c0001t0001g0211a0001c0001t0003g0018a0001c0004t0002g0128others(2): Show | 6 | HG02055.hp1 HG03209.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1406_-8-1395del others(12): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATAT others(7): Show |
T | 1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-1408_-8-1395del others(14): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566247
|
TTATATAT others(9): Show |
T | 4 | a0001c0002t0003g0029a0001c0027t0003g0282a0003c0007t0007g0281others(1): Show | 5 | HG02109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1410_-8-1395del others(16): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566247 | ||||||
chr16:20566251
|
A | T | 4 | a0006c0010t0003g0011a0006c0010t0003g0115a0006c0010t0003g0116others(1): Show | 5 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1398T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566251 | ||||||
chr16:20566253
|
A | T | 6 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(3): Show | 6 | HG01884.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1400T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566253 | ||||||
chr16:20566255
|
A | T | 4 | a0008c0013t0002g0106a0008c0013t0002g0107a0008c0013t0002g0108others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1402T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566255 | ||||||
chr16:20566257
|
A | T | 1 | a0006c0010t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-1404T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566257 | ||||||
chr16:20566286
|
G | T | 1 | a0002c0003t0010g0053 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-8-1433C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566286 | ||||||
chr16:20566388
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-8-1535T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566388 | ||||||
chr16:20566395
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-8-1542C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566395 | ||||||
chr16:20566404
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1551A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566404 | ||||||
chr16:20566422
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1569A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566422 | ||||||
chr16:20566423
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1570T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566423 | ||||||
chr16:20566424
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1571A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566424 | ||||||
chr16:20566425
|
T | C | 1 | a0001c0004t0007g0203 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-8-1572A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566425 | ||||||
chr16:20566461
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-1608A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566461 | ||||||
chr16:20566534
|
ATACTATA others(4): Show |
A | 1 | a0007c0014t0001g0155 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8-1692_-8-1682del others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566534 | ||||||
chr16:20566544
|
A | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-1691T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566544 | ||||||
chr16:20566545
|
C | G | 1 | a0001c0002t0004g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-1692G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566545 | ||||||
chr16:20566615
|
A | G | 4 | a0002c0003t0005g0044a0002c0003t0005g0046a0002c0003t0005g0051others(1): Show | 4 | NA18959.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1762T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566615 | ||||||
chr16:20566634
|
G | A | 1 | a0001c0002t0004g0279 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-1781C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566634 | ||||||
chr16:20566634
|
G | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 145 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-8-1781C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566634 | ||||||
chr16:20566635
|
T | C | 3 | a0001c0001t0023g0208a0003c0008t0011g0316a0003c0008t0011g0317 | 3 | HG02257.hp2 HG03139.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-8-1782A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566635 | ||||||
chr16:20566640
|
A | AC | 16 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(13): Show | 17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1788_-8-1787ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566640 | ||||||
chr16:20566640
|
ATATAC | A | 3 | a0001c0004t0002g0126a0002c0003t0005g0082a0003c0008t0011g0316 | 3 | HG02257.hp2 HG02809.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-8-1792_-8-1788del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566640 | ||||||
chr16:20566644
|
A | AGTATATA others(92): Show |
1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8-1792_-8-1791ins others(99): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566644 | ||||||
chr16:20566644
|
AC | A | 16 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(13): Show | 17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1792delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566644 | ||||||
chr16:20566645
|
C | A | 3 | a0001c0001t0001g0165a0001c0001t0003g0142a0001c0002t0007g0104 | 3 | HG02040.hp2 NA18972.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-8-1792G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATA | 105 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0001g0168others(102): Show | 113 | HG00597.hp1 HG00673.hp1 HG01099.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8-1796_-8-1793dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(24): Show |
1 | a0001c0001t0003g0015 | 2 | HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(31): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(83): Show |
1 | a0001c0001t0008g0337 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(101): Show |
1 | a0001c0004t0004g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(108): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(40): Show |
15 | a0001c0001t0003g0014a0001c0001t0003g0124a0001c0001t0003g0131others(12): Show | 17 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(47): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(83): Show |
14 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01515.hp2 HG01952.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(74): Show |
1 | a0001c0001t0018g0138 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(81): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(40): Show |
1 | a0005c0016t0016g0326 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(47): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(121): Show |
1 | a0005c0011t0008g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(128): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(26): Show |
1 | a0001c0001t0001g0210 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(33): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(103): Show |
1 | a0001c0004t0004g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(150): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0172a0001c0001t0001g0218others(1): Show | 5 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(157): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(69): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | HG02080.hp1 NA18945.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(76): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(103): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(54): Show | 70 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(137): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0170a0001c0004t0002g0171 | 8 | NA18956.hp1 NA18970.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(94): Show |
1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(101): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(103): Show |
4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0167others(1): Show | 4 | NA18951.hp2 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(110): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566645
|
C | CTATATAT others(83): Show |
1 | a0001c0001t0003g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-8-1793_-8-1792ins others(90): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566645 | ||||||
chr16:20566650
|
C | G | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-1797G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566650 | ||||||
chr16:20566656
|
A | ATAC | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-1804_-8-1803ins others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566656 | ||||||
chr16:20566658
|
A | AC | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG01361.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566658
|
A | ACTATATA others(1): Show |
5 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(2): Show | 6 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(8): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566658
|
A | AG | 46 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(43): Show | 48 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566658
|
A | AGTATATA others(98): Show |
1 | a0003c0008t0003g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(105): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566658
|
A | AGTATATA others(100): Show |
1 | a0003c0025t0003g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-8-1806_-8-1805ins others(107): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566658
|
AT | A | 102 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(99): Show | 112 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-1806delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566658 | ||||||
chr16:20566659
|
T | A | 7 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(4): Show | 8 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1806A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566659 | ||||||
chr16:20566659
|
T | TA | 8 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0001g0168others(5): Show | 8 | NA18950.hp1 NA18977.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1807_-8-1806ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566659 | ||||||
chr16:20566660
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 142 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-8-1807C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566660 | ||||||
chr16:20566660
|
G | C | 74 | a0001c0001t0001g0022a0001c0001t0001g0123a0001c0001t0001g0134others(71): Show | 79 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-8-1807C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566660 | ||||||
chr16:20566669
|
G | C | 91 | a0001c0001t0001g0022a0001c0001t0001g0168a0001c0001t0001g0169others(88): Show | 97 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(94): Show |
intron_variant | MODIFIER | c.-8-1816C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566669 | ||||||
chr16:20566669
|
G | T | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1816C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566669 | ||||||
chr16:20566670
|
T | A | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1817A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566670 | ||||||
chr16:20566671
|
A | C | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1818T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566671 | ||||||
chr16:20566672
|
TATAC | T | 9 | a0001c0002t0003g0112a0001c0006t0011g0110a0006c0010t0003g0114others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1823_-8-1820del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566672 | ||||||
chr16:20566673
|
A | ATATAC | 47 | a0001c0001t0003g0145a0001c0002t0002g0111a0002c0003t0005g0009others(44): Show | 51 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATACTA others(156): Show |
1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(163): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATACTA others(127): Show |
1 | a0002c0003t0013g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(134): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATACTA others(129): Show |
9 | a0002c0003t0010g0053a0002c0009t0009g0010a0002c0009t0009g0054others(6): Show | 10 | HG02074.hp2 HG03491.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(136): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATACTA others(158): Show |
1 | a0002c0009t0009g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATAG | 6 | a0003c0008t0011g0317a0005c0011t0026g0327a0008c0013t0002g0106others(3): Show | 6 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATAGTA others(144): Show |
3 | a0003c0007t0014g0340a0003c0007t0014g0341a0003c0007t0014g0343 | 3 | HG02258.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(151): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATAGTA others(171): Show |
3 | a0003c0008t0001g0319a0003c0008t0015g0031a0003c0008t0015g0318 | 4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(178): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATAGTA others(146): Show |
1 | a0003c0007t0014g0342 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(153): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATATAC others(127): Show |
5 | a0004c0005t0006g0045a0004c0005t0006g0086a0004c0005t0006g0088others(2): Show | 5 | HG01099.hp2 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(134): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATATAC others(410): Show |
1 | a0004c0005t0006g0087 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(417): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566673
|
A | ATATATAC others(105): Show |
1 | a0004c0005t0006g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1821_-8-1820ins others(112): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566673 | ||||||
chr16:20566674
|
TAC | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0210a0001c0004t0002g0126others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1823_-8-1822del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566674 | ||||||
chr16:20566676
|
C | CTAT | 6 | a0001c0001t0001g0158a0002c0003t0005g0050a0003c0007t0007g0229others(3): Show | 6 | HG00741.hp2 HG02451.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566676
|
C | CTATATAT others(12): Show |
1 | a0012c0030t0018g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(19): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566676
|
C | CTATATAT others(240): Show |
1 | a0006c0020t0003g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(247): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566676
|
C | CTATATAT others(267): Show |
1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-1824_-8-1823ins others(274): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566676
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(196): Show | 226 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.-8-1823G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566676
|
CATAT | C | 15 | a0001c0001t0003g0014a0001c0001t0003g0124a0001c0001t0003g0131others(12): Show | 17 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-1827_-8-1824del others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566676 | ||||||
chr16:20566678
|
T | C | 1 | a0001c0002t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-1825A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566678 | ||||||
chr16:20566679
|
A | ACTATATA others(67): Show |
12 | a0004c0005t0006g0040a0004c0005t0006g0093a0004c0005t0006g0094others(9): Show | 12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-1827_-8-1826ins others(74): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566679 | ||||||
chr16:20566680
|
T | C | 22 | a0001c0001t0001g0022a0001c0001t0001g0168a0001c0001t0001g0169others(19): Show | 23 | HG01099.hp2 HG01884.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1827A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | ||||||
chr16:20566680
|
T | G | 2 | a0003c0008t0011g0320a0003c0008t0011g0321 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-1827A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | ||||||
chr16:20566680
|
T | TC | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 110 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-8-1828_-8-1827ins others(1): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566680 | ||||||
chr16:20566681
|
A | ACTATATG others(4): Show |
1 | a0005c0016t0016g0326 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-1829_-8-1828ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | ||||||
chr16:20566681
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 146 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8-1828T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | ||||||
chr16:20566681
|
AG | A | 12 | a0004c0005t0006g0040a0004c0005t0006g0093a0004c0005t0006g0094others(9): Show | 12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-1829delC | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566681 | ||||||
chr16:20566682
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(109): Show | 134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-1829C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | C | 10 | a0001c0001t0001g0158a0001c0002t0003g0112a0001c0006t0011g0110others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-1829C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTA | 14 | a0002c0003t0010g0053a0002c0003t0013g0049a0002c0009t0009g0010others(11): Show | 15 | HG02055.hp2 HG02074.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1831_-8-1830dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAC others(45): Show |
4 | a0005c0016t0029g0324a0009c0015t0008g0032a0009c0015t0008g0329others(1): Show | 5 | HG02630.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(52): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAC others(115): Show |
8 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0254others(5): Show | 11 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(122): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAC others(140): Show |
1 | a0001c0002t0002g0253 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(147): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(4): Show |
2 | a0003c0008t0011g0317a0006c0010t0003g0011 | 3 | HG02895.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(99): Show |
1 | a0003c0007t0007g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(106): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(79): Show |
2 | a0002c0003t0005g0081a0002c0003t0010g0083 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(106): Show |
2 | a0002c0003t0013g0047a0002c0003t0013g0048 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(113): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(140): Show |
3 | a0002c0003t0005g0078a0002c0003t0013g0079a0002c0029t0010g0080 | 3 | HG01256.hp1 HG01257.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(147): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(108): Show |
21 | a0002c0003t0005g0009a0002c0003t0005g0042a0002c0003t0005g0043others(18): Show | 22 | HG00673.hp1 HG01891.hp2 HG02886.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(115): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(137): Show |
3 | a0002c0003t0005g0044a0002c0003t0005g0072a0002c0003t0005g0074 | 3 | HG01975.hp2 NA18954.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(166): Show |
3 | a0002c0003t0005g0077a0002c0009t0009g0076a0002c0018t0005g0075 | 3 | HG02040.hp1 HG03710.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(173): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566682
|
G | GTATATAT others(119): Show |
1 | a0002c0003t0005g0041 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-8-1830_-8-1829ins others(126): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566682 | ||||||
chr16:20566689
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1836G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | ||||||
chr16:20566689
|
C | G | 2 | a0003c0008t0011g0316a0003c0008t0011g0317 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1836G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | ||||||
chr16:20566689
|
C | T | 9 | a0001c0002t0003g0112a0001c0006t0011g0110a0006c0010t0003g0114others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1836G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566689 | ||||||
chr16:20566690
|
T | A | 9 | a0001c0002t0003g0112a0001c0006t0011g0110a0006c0010t0003g0114others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1837A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566690 | ||||||
chr16:20566691
|
A | G | 9 | a0001c0002t0003g0112a0001c0006t0011g0110a0006c0010t0003g0114others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1838T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566691 | ||||||
chr16:20566697
|
AGT | A | 29 | a0001c0001t0001g0210a0001c0001t0003g0014a0001c0001t0003g0124others(26): Show | 31 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-1846_-8-1845del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566697 | ||||||
chr16:20566698
|
G | A | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1845C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | ||||||
chr16:20566698
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 130 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-8-1845C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | ||||||
chr16:20566698
|
GTA | G | 15 | a0001c0002t0004g0305a0001c0002t0022g0309a0001c0006t0001g0306others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1847_-8-1846del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566698 | ||||||
chr16:20566700
|
A | ATATAC | 4 | a0001c0004t0002g0126a0002c0003t0010g0004a0002c0018t0010g0039others(1): Show | 7 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC | 16 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0207others(13): Show | 17 | HG02074.hp2 HG02486.hp1 HG03130.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(25): Show |
4 | a0008c0013t0002g0106a0008c0013t0002g0107a0008c0013t0002g0108others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(32): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(27): Show |
2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(34): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(16): Show |
1 | a0004c0005t0006g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(23): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(18): Show |
43 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(40): Show | 44 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(25): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(43): Show |
2 | a0002c0003t0005g0084a0002c0003t0010g0083 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(50): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(88): Show |
3 | a0001c0002t0004g0227a0001c0002t0004g0300a0001c0006t0001g0299 | 3 | HG03688.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(95): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(113): Show |
2 | a0001c0012t0007g0024a0001c0012t0007g0223 | 3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAC others(138): Show |
1 | a0001c0002t0002g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG | 8 | a0001c0001t0001g0168a0001c0001t0001g0169a0003c0007t0014g0340others(5): Show | 9 | HG02258.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(109): Show |
1 | a0001c0006t0003g0313 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(116): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(185): Show |
1 | a0001c0002t0004g0270 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(192): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(151): Show |
3 | a0001c0002t0003g0260a0001c0002t0003g0261a0001c0002t0004g0297 | 3 | HG02451.hp2 NA18964.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(158): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(50): Show |
1 | a0001c0001t0001g0022 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(57): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(147): Show |
2 | a0005c0024t0016g0334a0010c0022t0008g0325 | 2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(154): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(210): Show |
1 | a0005c0011t0026g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(217): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(113): Show |
1 | a0001c0002t0004g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(95): Show |
1 | a0005c0016t0029g0324 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(102): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(79): Show |
2 | a0005c0016t0016g0326a0010c0023t0027g0332 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(133): Show |
2 | a0005c0011t0019g0033a0005c0016t0028g0333 | 3 | HG01891.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(140): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(153): Show |
2 | a0003c0008t0011g0320a0003c0008t0011g0321 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(160): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(134): Show |
1 | a0001c0002t0002g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(141): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(113): Show |
16 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(13): Show | 16 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(70): Show |
1 | a0001c0002t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(77): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(104): Show |
1 | a0001c0002t0002g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(113): Show |
25 | a0001c0002t0002g0228a0001c0002t0002g0249a0001c0002t0002g0250others(22): Show | 27 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(138): Show |
7 | a0001c0002t0002g0244a0001c0002t0002g0246a0001c0002t0002g0247others(4): Show | 7 | HG00735.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(172): Show |
1 | a0001c0002t0002g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(179): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(160): Show |
2 | a0001c0002t0004g0311a0001c0002t0004g0312 | 2 | HG02083.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(167): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(122): Show |
1 | a0001c0002t0004g0271 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(129): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(104): Show |
1 | a0001c0002t0003g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(113): Show |
16 | a0001c0002t0004g0003a0001c0002t0004g0027a0001c0002t0004g0220others(13): Show | 21 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(138): Show |
1 | a0001c0002t0021g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(138): Show |
2 | a0001c0002t0004g0266a0001c0002t0004g0304 | 2 | HG01167.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(145): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(113): Show |
1 | a0001c0017t0004g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(120): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(104): Show |
1 | a0001c0002t0004g0298 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(144): Show |
1 | a0001c0002t0004g0301 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(151): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(171): Show |
1 | a0001c0002t0004g0028 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(178): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAG others(60): Show |
1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(67): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-1848_-8-1847ins others(10): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566700
|
A | C | 29 | a0001c0001t0001g0210a0001c0001t0003g0014a0001c0001t0003g0124others(26): Show | 31 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-1847T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566700 | ||||||
chr16:20566702
|
A | ATATACTA others(68): Show |
1 | a0001c0002t0002g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8-1850_-8-1849ins others(75): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566702 | ||||||
chr16:20566703
|
T | A | 1 | a0004c0005t0006g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1850A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | ||||||
chr16:20566703
|
T | TATAGTAT others(104): Show |
2 | a0009c0015t0008g0032a0009c0015t0008g0329 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(111): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | ||||||
chr16:20566703
|
T | TATAGTAT others(36): Show |
1 | a0005c0011t0008g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(43): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | ||||||
chr16:20566703
|
T | TATAGTAT others(158): Show |
2 | a0005c0011t0008g0330a0005c0011t0008g0331 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8-1851_-8-1850ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566703 | ||||||
chr16:20566707
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(91): Show | 114 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-8-1854A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566707 | ||||||
chr16:20566709
|
G | C | 46 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0003g0014others(43): Show | 52 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.-8-1856C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566709 | ||||||
chr16:20566712
|
T | C | 1 | a0004c0005t0006g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-1859A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566712 | ||||||
chr16:20566716
|
T | C | 57 | a0001c0001t0003g0145a0001c0002t0002g0111a0001c0002t0004g0266others(54): Show | 59 | HG00597.hp1 HG00673.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.-8-1863A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | ||||||
chr16:20566716
|
T | TACTATAT others(79): Show |
14 | a0001c0002t0003g0112a0001c0006t0011g0110a0006c0010t0003g0011others(11): Show | 15 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1864_-8-1863ins others(86): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | ||||||
chr16:20566716
|
T | TAGTATAT others(2): Show |
7 | a0002c0003t0010g0053a0004c0005t0006g0045a0004c0005t0006g0086others(4): Show | 7 | HG01099.hp2 HG01884.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1872_-8-1864dup others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566716 | ||||||
chr16:20566717
|
A | ACT | 4 | a0002c0003t0005g0084a0002c0003t0010g0083a0006c0020t0003g0105others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1865_-8-1864ins others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566717 | ||||||
chr16:20566717
|
A | T | 4 | a0001c0001t0003g0145a0001c0002t0004g0266a0001c0002t0004g0303others(1): Show | 4 | HG00323.hp2 HG00597.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1864T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566717 | ||||||
chr16:20566718
|
G | A | 7 | a0001c0002t0004g0266a0001c0002t0004g0303a0001c0002t0004g0304others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1865C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0003g0142others(1): Show | 4 | HG02809.hp2 NA18972.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1865C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTA | 15 | a0001c0002t0003g0262a0002c0003t0005g0081a0003c0007t0007g0322others(12): Show | 16 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-1867_-8-1866dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAC others(18): Show |
1 | a0001c0002t0004g0323 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8-1890_-8-1866dup others(25): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(304): Show |
1 | a0001c0002t0003g0012 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(304): Show |
2 | a0003c0007t0003g0119a0003c0007t0003g0120 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(304): Show |
1 | a0016c0028t0003g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(311): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(31): Show |
2 | a0001c0006t0001g0306a0001c0006t0001g0307 | 2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(38): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(56): Show |
1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(63): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566718
|
G | GTATATAT others(165): Show |
1 | a0001c0002t0004g0305 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-1866_-8-1865ins others(172): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566718 | ||||||
chr16:20566722
|
A | G | 1 | a0001c0004t0004g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-1869T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566722 | ||||||
chr16:20566723
|
T | TATAC | 3 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0003g0142 | 3 | NA18972.hp1 NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-8-1871_-8-1870ins others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566723 | ||||||
chr16:20566723
|
T | TATATATC others(27): Show |
16 | a0001c0001t0003g0014a0001c0001t0003g0124a0001c0001t0003g0131others(13): Show | 18 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1871_-8-1870ins others(34): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566723 | ||||||
chr16:20566725
|
C | CTATATAT others(4): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-8-1873_-8-1872ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | ||||||
chr16:20566725
|
C | G | 22 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0003g0014others(19): Show | 24 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8-1872G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | ||||||
chr16:20566725
|
C | T | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-1872G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566725 | ||||||
chr16:20566726
|
T | A | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-1873A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566726 | ||||||
chr16:20566727
|
A | G | 2 | a0001c0004t0002g0126a0003c0008t0011g0316 | 2 | HG02257.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-8-1874T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566727 | ||||||
chr16:20566732
|
T | C | 1 | a0001c0002t0003g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1879A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566732 | ||||||
chr16:20566733
|
A | ATT | 3 | a0003c0007t0003g0119a0003c0007t0003g0120a0016c0028t0003g0118 | 3 | HG02486.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-8-1881_-8-1880ins others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566733 | ||||||
chr16:20566733
|
A | T | 1 | a0001c0002t0003g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-1880T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566733 | ||||||
chr16:20566734
|
G | A | 8 | a0001c0002t0003g0262a0001c0004t0002g0126a0002c0003t0005g0082others(5): Show | 10 | HG01081.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1881C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(97): Show | 120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-1881C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTA | 69 | a0001c0002t0002g0111a0001c0002t0003g0012a0001c0002t0003g0112others(66): Show | 73 | HG00673.hp1 HG01256.hp1 HG01257.hp1 others(70): Show |
intron_variant | MODIFIER | c.-8-1883_-8-1882dup others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTATA | 3 | a0003c0008t0001g0319a0003c0008t0015g0031a0003c0008t0015g0318 | 4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1885_-8-1882dup others(4): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTATATAC others(56): Show |
1 | a0002c0003t0005g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(63): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTATATAC others(95): Show |
2 | a0001c0006t0001g0306a0001c0006t0001g0307 | 2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(102): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTATATAT others(164): Show |
1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(171): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566734
|
G | GTATATAT others(137): Show |
1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1882_-8-1881ins others(144): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566734 | ||||||
chr16:20566735
|
TATATA | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 112 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-1887_-8-1883del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566735 | ||||||
chr16:20566740
|
A | ATACTATA others(70): Show |
1 | a0001c0001t0003g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(77): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | ||||||
chr16:20566740
|
A | ATACTATA others(76): Show |
1 | a0001c0001t0001g0210 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(83): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | ||||||
chr16:20566740
|
A | ATAGTATA others(110): Show |
6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0204others(3): Show | 6 | NA18950.hp1 NA18989.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1888_-8-1887ins others(117): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566740 | ||||||
chr16:20566741
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(97): Show | 120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-1888G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566741 | ||||||
chr16:20566750
|
C | CTATATAT others(2): Show |
14 | a0001c0002t0007g0104a0005c0011t0008g0328a0005c0011t0008g0330others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-1906_-8-1898dup others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | ||||||
chr16:20566750
|
C | CTGTATAT others(4): Show |
21 | a0001c0001t0001g0022a0001c0001t0001g0158a0001c0001t0001g0159others(18): Show | 23 | HG00597.hp2 HG00673.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8-1898_-8-1897ins others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | ||||||
chr16:20566750
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 130 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-8-1897G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566750 | ||||||
chr16:20566758
|
A | AGTATATA others(9): Show |
1 | a0001c0004t0002g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8-1906_-8-1905ins others(16): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566758 | ||||||
chr16:20566759
|
G | C | 5 | a0002c0003t0005g0081a0003c0007t0007g0322a0003c0008t0011g0316others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1906C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | ||||||
chr16:20566759
|
G | GTATATAC others(158): Show |
1 | a0002c0003t0005g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(165): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | ||||||
chr16:20566759
|
G | GTATATAT others(2): Show |
89 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(86): Show | 93 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(9): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | ||||||
chr16:20566759
|
G | GTATATAT others(180): Show |
2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1907_-8-1906ins others(187): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | ||||||
chr16:20566759
|
G | T | 4 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1906C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566759 | ||||||
chr16:20566920
|
A | T | 1 | a0002c0003t0005g0044 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8-2067T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566920 | ||||||
chr16:20566937
|
A | T | 29 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(26): Show | 31 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-2084T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566937 | ||||||
chr16:20566952
|
ATATATAT | A | 16 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0002t0007g0104others(13): Show | 17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-2106_-8-2100del others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20566952 | ||||||
chr16:20567070
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 273 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(270): Show |
intron_variant | MODIFIER | c.-8-2217A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567070 | ||||||
chr16:20567249
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-2396A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567249 | ||||||
chr16:20567346
|
AATATATT | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-8-2500_-8-2494del others(7): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567346 | ||||||
chr16:20567381
|
TATA | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2531_-8-2529del others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567381 | ||||||
chr16:20567396
|
A | G | 1 | a0010c0023t0027g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-2543T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567396 | ||||||
chr16:20567405
|
T | C | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-8-2552A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567405 | ||||||
chr16:20567416
|
T | C | 1 | a0001c0004t0004g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-2563A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567416 | ||||||
chr16:20567463
|
TATA | T | 5 | a0001c0002t0007g0224a0001c0002t0007g0230a0001c0002t0007g0231others(2): Show | 5 | HG00639.hp2 HG00741.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2613_-8-2611del others(3): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567463 | ||||||
chr16:20567493
|
A | AATATATA others(4): Show |
235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 268 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.-8-2651_-8-2641dup others(11): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567493 | ||||||
chr16:20567510
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2657T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567510 | ||||||
chr16:20567512
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2659A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567512 | ||||||
chr16:20567520
|
A | AAAGTAAT others(6): Show |
1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-2668_-8-2667ins others(13): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567520 | ||||||
chr16:20567522
|
A | G | 1 | a0008c0013t0002g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-2669T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567522 | ||||||
chr16:20567531
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-2678T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567531 | ||||||
chr16:20567619
|
G | A | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-2766C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567619 | ||||||
chr16:20567642
|
A | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2789T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567642 | ||||||
chr16:20567645
|
C | G | 97 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(94): Show | 103 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(100): Show |
intron_variant | MODIFIER | c.-8-2792G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567645 | ||||||
chr16:20567669
|
C | G | 1 | a0001c0002t0004g0267 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-8-2816G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567669 | ||||||
chr16:20567669
|
C | T | 8 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-2816G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567669 | ||||||
chr16:20567684
|
A | G | 1 | a0001c0002t0003g0263 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8-2831T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567684 | ||||||
chr16:20567698
|
A | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-2845T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567698 | ||||||
chr16:20567731
|
G | C | 1 | a0001c0002t0004g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-2878C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567731 | ||||||
chr16:20567808
|
T | C | 1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-2955A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567808 | ||||||
chr16:20567823
|
T | C | 1 | a0001c0002t0002g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-2970A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567823 | ||||||
chr16:20567973
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(81): Show | 104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-8-3120A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20567973 | ||||||
chr16:20568083
|
A | G | 1 | a0001c0001t0001g0017 | 2 | NA18989.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-3230T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568083 | ||||||
chr16:20568286
|
T | C | 1 | a0004c0005t0006g0103 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8-3433A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568286 | ||||||
chr16:20568335
|
TATATA | T | 35 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(32): Show | 39 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8-3487_-8-3483del others(5): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568335 | ||||||
chr16:20568341
|
A | T | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-3488T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568341 | ||||||
chr16:20568342
|
T | C | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-8-3489A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568342 | ||||||
chr16:20568344
|
T | C | 1 | a0003c0008t0011g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-3491A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568344 | ||||||
chr16:20568350
|
A | T | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-3497T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568350 | ||||||
chr16:20568444
|
T | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-3591A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568444 | ||||||
chr16:20568470
|
T | C | 1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-3617A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568470 | ||||||
chr16:20568484
|
G | C | 1 | a0001c0002t0002g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-3631C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568484 | ||||||
chr16:20568611
|
G | T | 3 | a0003c0008t0001g0319a0003c0008t0015g0031a0003c0008t0015g0318 | 4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3758C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568611 | ||||||
chr16:20568627
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-8-3774A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568627 | ||||||
chr16:20568904
|
T | C | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-4051A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20568904 | ||||||
chr16:20569030
|
G | T | 1 | a0001c0017t0004g0026 | 2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-8-4177C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569030 | ||||||
chr16:20569042
|
C | T | 1 | a0001c0001t0003g0157 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-8-4189G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569042 | ||||||
chr16:20569090
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-8-4237G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569090 | ||||||
chr16:20569328
|
C | T | 1 | a0001c0004t0002g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-8-4475G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569328 | ||||||
chr16:20569357
|
G | A | 1 | a0004c0005t0006g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4504C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569357 | ||||||
chr16:20569431
|
C | T | 1 | a0001c0002t0003g0012 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-4578G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569431 | ||||||
chr16:20569499
|
G | A | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-4646C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569499 | ||||||
chr16:20569519
|
T | G | 2 | a0002c0003t0010g0004a0002c0018t0010g0039 | 4 | HG02559.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-4666A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569519 | ||||||
chr16:20569530
|
G | C | 1 | a0001c0002t0022g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-4677C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569530 | ||||||
chr16:20569566
|
G | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0218a0001c0004t0007g0217 | 4 | NA18943.hp1 NA19002.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-4713C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569566 | ||||||
chr16:20569594
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(318): Show | 363 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(360): Show |
intron_variant | MODIFIER | c.-8-4741G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569594 | ||||||
chr16:20569648
|
G | C | 1 | a0001c0002t0002g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-4795C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569648 | ||||||
chr16:20569791
|
G | C | 1 | a0002c0003t0005g0085 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-8-4938C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569791 | ||||||
chr16:20569878
|
A | G | 1 | a0002c0003t0005g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8-5025T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20569878 | ||||||
chr16:20570006
|
C | G | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8-5153G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570006 | ||||||
chr16:20570010
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8-5157T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570010 | ||||||
chr16:20570266
|
T | C | 1 | a0003c0007t0004g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8-5413A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570266 | ||||||
chr16:20570294
|
C | T | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-5441G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570294 | ||||||
chr16:20570322
|
G | T | 1 | a0002c0003t0005g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-8-5469C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570322 | ||||||
chr16:20570509
|
G | T | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-5656C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570509 | ||||||
chr16:20570534
|
C | T | 1 | a0001c0002t0002g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-9+5673G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570534 | ||||||
chr16:20570551
|
G | C | 15 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(12): Show | 16 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+5656C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570551 | ||||||
chr16:20570721
|
A | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+5486T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570721 | ||||||
chr16:20570796
|
C | G | 3 | a0001c0001t0008g0335a0001c0001t0008g0336a0001c0001t0008g0337 | 3 | HG02155.hp1 NA18612.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-9+5411G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570796 | ||||||
chr16:20570800
|
G | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+5407C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570800 | ||||||
chr16:20570962
|
TC | T | 10 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(7): Show | 11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+5244delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570962 | ||||||
chr16:20570963
|
C | T | 2 | a0003c0008t0011g0320a0003c0008t0011g0321 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+5244G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20570963 | ||||||
chr16:20571276
|
G | A | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4931C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571276 | ||||||
chr16:20571363
|
T | C | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4844A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571363 | ||||||
chr16:20571371
|
T | C | 1 | a0003c0008t0011g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+4836A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571371 | ||||||
chr16:20571509
|
A | C | 8 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+4698T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571509 | ||||||
chr16:20571539
|
A | G | 1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+4668T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571539 | ||||||
chr16:20571540
|
T | C | 3 | a0001c0002t0002g0257a0001c0002t0002g0258a0001c0002t0002g0259 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-9+4667A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571540 | ||||||
chr16:20571550
|
G | T | 1 | a0001c0004t0002g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-9+4657C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571550 | ||||||
chr16:20571597
|
G | A | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+4610C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571597 | ||||||
chr16:20571646
|
C | A | 1 | a0010c0023t0027g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4561G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571646 | ||||||
chr16:20571756
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-9+4451T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571756 | ||||||
chr16:20571870
|
G | T | 13 | a0005c0011t0008g0328a0005c0011t0008g0330a0005c0011t0008g0331others(10): Show | 15 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+4337C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571870 | ||||||
chr16:20571916
|
G | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+4291C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20571916 | ||||||
chr16:20572060
|
A | G | 36 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(33): Show | 40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+4147T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572060 | ||||||
chr16:20572238
|
G | C | 1 | a0001c0004t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9+3969C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572238 | ||||||
chr16:20572238
|
G | T | 68 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(65): Show | 72 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.-9+3969C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572238 | ||||||
chr16:20572267
|
C | A | 12 | a0004c0005t0006g0092a0004c0005t0006g0093a0004c0005t0006g0094others(9): Show | 12 | HG01934.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+3940G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572267 | ||||||
chr16:20572460
|
T | C | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+3747A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572460 | ||||||
chr16:20572490
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(222): Show | 256 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.-9+3717A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572490 | ||||||
chr16:20572509
|
C | T | 1 | a0001c0002t0003g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9+3698G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572509 | ||||||
chr16:20572572
|
A | G | 3 | a0001c0002t0004g0264a0001c0002t0004g0265a0001c0002t0004g0266 | 3 | HG01167.hp2 HG02683.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+3635T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572572 | ||||||
chr16:20572633
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9+3574A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572633 | ||||||
chr16:20572664
|
T | C | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+3543A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572664 | ||||||
chr16:20572667
|
A | G | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9+3540T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572667 | ||||||
chr16:20572774
|
A | T | 67 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(64): Show | 71 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+3433T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572774 | ||||||
chr16:20572775
|
T | A | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+3432A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572775 | ||||||
chr16:20572965
|
A | C | 1 | a0001c0001t0001g0001 | 6 | NA18970.hp1 NA18972.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3242T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572965 | ||||||
chr16:20572974
|
A | AT | 66 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0002t0003g0262others(63): Show | 71 | HG00673.hp1 HG01081.hp2 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+3232dupA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | ||||||
chr16:20572974
|
AT | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 156 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-9+3232delA | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | ||||||
chr16:20572974
|
ATT | A | 9 | a0001c0002t0003g0012a0001c0004t0002g0144a0003c0007t0003g0119others(6): Show | 11 | HG00597.hp2 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+3231_-9+3232del others(2): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572974 | ||||||
chr16:20572978
|
T | C | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+3229A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572978 | ||||||
chr16:20572980
|
T | C | 6 | a0001c0002t0003g0012a0003c0007t0003g0119a0003c0007t0003g0120others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+3227A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20572980 | ||||||
chr16:20573003
|
C | A | 1 | a0001c0004t0002g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-9+3204G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573003 | ||||||
chr16:20573005
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 157 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-9+3202G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573005 | ||||||
chr16:20573108
|
A | G | 2 | a0001c0002t0003g0260a0001c0002t0003g0261 | 2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+3099T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573108 | ||||||
chr16:20573119
|
T | G | 3 | a0003c0008t0001g0319a0003c0008t0015g0031a0003c0008t0015g0318 | 4 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3088A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573119 | ||||||
chr16:20573140
|
C | T | 1 | a0007c0014t0001g0155 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-9+3067G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573140 | ||||||
chr16:20573172
|
T | A | 5 | a0001c0001t0001g0147a0001c0001t0003g0145a0001c0001t0003g0146others(2): Show | 6 | HG00597.hp1 HG00621.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3035A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573172 | ||||||
chr16:20573310
|
G | T | 1 | a0001c0001t0003g0125 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-9+2897C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573310 | ||||||
chr16:20573363
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+2844C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573363 | ||||||
chr16:20573418
|
T | G | 1 | a0001c0002t0007g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9+2789A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573418 | ||||||
chr16:20573459
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(215): Show | 248 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(245): Show |
intron_variant | MODIFIER | c.-9+2748A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573459 | ||||||
chr16:20573525
|
G | T | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+2682C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573525 | ||||||
chr16:20573528
|
T | A | 139 | a0001c0002t0002g0288a0001c0002t0002g0291a0001c0002t0002g0302others(136): Show | 151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9+2679A>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573528 | ||||||
chr16:20573661
|
G | C | 1 | a0003c0007t0007g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+2546C>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573661 | ||||||
chr16:20573681
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(81): Show | 104 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-9+2526G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573681 | ||||||
chr16:20573759
|
G | A | 1 | a0001c0002t0007g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+2448C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573759 | ||||||
chr16:20573822
|
A | T | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+2385T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573822 | ||||||
chr16:20573890
|
A | G | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+2317T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573890 | ||||||
chr16:20573940
|
T | C | 1 | a0001c0006t0003g0313 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-9+2267A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573940 | ||||||
chr16:20573993
|
G | A | 1 | a0005c0024t0016g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-9+2214C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20573993 | ||||||
chr16:20574052
|
C | T | 1 | a0001c0002t0004g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+2155G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574052 | ||||||
chr16:20574054
|
A | G | 4 | a0001c0001t0001g0154a0001c0006t0003g0225a0001c0006t0003g0226others(1): Show | 4 | HG00609.hp2 NA18961.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2153T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574054 | ||||||
chr16:20574130
|
C | T | 1 | a0001c0002t0007g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9+2077G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574130 | ||||||
chr16:20574145
|
A | G | 2 | a0001c0012t0007g0024a0001c0012t0007g0223 | 3 | HG02965.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-9+2062T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574145 | ||||||
chr16:20574242
|
G | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+1965C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574242 | ||||||
chr16:20574309
|
C | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+1898G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574309 | ||||||
chr16:20574311
|
G | A | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+1896C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574311 | ||||||
chr16:20574358
|
T | C | 2 | a0003c0008t0003g0122a0003c0025t0003g0121 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-9+1849A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574358 | ||||||
chr16:20574617
|
C | T | 1 | a0006c0020t0020g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+1590G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574617 | ||||||
chr16:20574689
|
C | T | 69 | a0001c0002t0007g0104a0002c0003t0005g0009a0002c0003t0005g0041others(66): Show | 73 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+1518G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574689 | ||||||
chr16:20574860
|
T | C | 14 | a0001c0001t0003g0124a0001c0004t0002g0149a0003c0007t0007g0322others(11): Show | 15 | HG01168.hp2 HG02055.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+1347A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574860 | ||||||
chr16:20574862
|
G | T | 13 | a0001c0001t0003g0124a0003c0007t0007g0322a0003c0007t0014g0340others(10): Show | 14 | HG02055.hp2 HG02056.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+1345C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574862 | ||||||
chr16:20574871
|
A | T | 1 | a0001c0002t0002g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-9+1336T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574871 | ||||||
chr16:20574876
|
C | T | 1 | a0003c0008t0011g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+1331G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574876 | ||||||
chr16:20574917
|
A | T | 1 | a0002c0003t0005g0041 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9+1290T>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574917 | ||||||
chr16:20574949
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 247 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-9+1258T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20574949 | ||||||
chr16:20575140
|
G | T | 12 | a0003c0007t0007g0322a0003c0007t0014g0340a0003c0007t0014g0341others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+1067C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575140 | ||||||
chr16:20575174
|
G | GAACTCCA others(12): Show |
2 | a0001c0004t0002g0150a0001c0004t0002g0151 | 2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-9+1014_-9+1032dup others(19): Show |
ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575174 | ||||||
chr16:20575200
|
T | G | 94 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(91): Show | 98 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9+1007A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575200 | ||||||
chr16:20575297
|
A | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+910T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575297 | ||||||
chr16:20575331
|
A | G | 1 | a0001c0002t0007g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+876T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575331 | ||||||
chr16:20575338
|
T | G | 1 | a0001c0006t0003g0314 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-9+869A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575338 | ||||||
chr16:20575464
|
GC | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+742delG | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575464 | ||||||
chr16:20575465
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(217): Show | 252 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.-9+742G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575465 | ||||||
chr16:20575476
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA18951.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-9+731T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575476 | ||||||
chr16:20575534
|
A | C | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+673T>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575534 | ||||||
chr16:20575538
|
C | T | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+669G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575538 | ||||||
chr16:20575597
|
C | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 254 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-9+610G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575597 | ||||||
chr16:20575629
|
G | T | 1 | a0001c0002t0004g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-9+578C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575629 | ||||||
chr16:20575714
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 144 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+493G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575714 | ||||||
chr16:20575741
|
A | G | 4 | a0003c0007t0014g0340a0003c0007t0014g0341a0003c0007t0014g0342others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+466T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575741 | ||||||
chr16:20575784
|
C | G | 36 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0135others(33): Show | 40 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+423G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575784 | ||||||
chr16:20575797
|
T | G | 66 | a0002c0003t0005g0009a0002c0003t0005g0041a0002c0003t0005g0042others(63): Show | 68 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9+410A>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575797 | ||||||
chr16:20575806
|
A | G | 17 | a0001c0002t0002g0111a0001c0002t0003g0112a0001c0006t0011g0110others(14): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+401T>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575806 | ||||||
chr16:20575809
|
G | T | 2 | a0006c0020t0003g0105a0006c0020t0020g0034 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9+398C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575809 | ||||||
chr16:20575874
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-9+333C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575874 | ||||||
chr16:20575932
|
G | A | 1 | a0001c0002t0002g0315 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-9+275C>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575932 | ||||||
chr16:20575969
|
C | A | 26 | a0001c0002t0007g0104a0003c0007t0007g0322a0003c0007t0014g0340others(23): Show | 29 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+238G>T | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20575969 | ||||||
chr16:20576003
|
T | C | 1 | a0001c0002t0004g0323 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+204A>G | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576003 | ||||||
chr16:20576024
|
C | G | 91 | a0001c0002t0002g0111a0001c0002t0003g0012a0001c0002t0003g0112others(88): Show | 97 | HG00673.hp1 HG01099.hp2 HG01256.hp1 others(94): Show |
intron_variant | MODIFIER | c.-9+183G>C | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576024 | ||||||
chr16:20576039
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G | T | 1 | a0001c0002t0007g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+168C>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576039 | ||||||
chr16:20576204
|
C | T | 13 | a0005c0011t0008g0328a0005c0011t0008g0330a0005c0011t0008g0331others(10): Show | 15 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-9+3G>A | ACSM2B | ENSG00000066813.14 | transcript | ENST00000329697.10 | protein_coding | 1/13 | chr16 | 20576204 |