geneid | 51205 |
---|---|
ensemblid | ENSG00000162836.12 |
hgncid | 29609 |
symbol | ACP6 |
name | acid phosphatase 6, lysophosphatidic |
refseq_nuc | NM_016361.5 |
refseq_prot | NP_057445.4 |
ensembl_nuc | ENST00000583509.7 |
ensembl_prot | ENSP00000463574.1 |
mane_status | MANE Select |
chr | chr1 |
start | 147642230 |
end | 147670524 |
strand | - |
ver | v1.2 |
region | chr1:147642230-147670524 |
region5000 | chr1:147637230-147675524 |
regionname0 | ACP6_chr1_147642230_147670524 |
regionname5000 | ACP6_chr1_147637230_147675524 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 428 | 387 | 76 | 61 | 194 | 14 | 40 | 146 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0002 | 0/0 | 428 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0003 | 0/0 | 428 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0004 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0005 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0006 | 0/0 | 428 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
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 | 0/1 | 1287 | 177 | 38 | 34 | 79 | 8 | 17 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0002 | 1/0 | 1287 | 101 | 11 | 17 | 54 | 4 | 14 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0003 | 0/0 | 1287 | 101 | 22 | 7 | 61 | 2 | 9 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0004 | 0/0 | 1287 | 11 | 11 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0005 | 0/0 | 1287 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0006 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0007 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0008 | 0/0 | 1287 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0009 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0010 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0011 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0012 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0013 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
c0014 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5673 | 75 | 20 | 12 | 36 | 2 | 5 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0002 | 0/0 | 5673 | 64 | 5 | 12 | 33 | 3 | 11 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0003 | 0/0 | 5673 | 62 | 0 | 5 | 51 | 2 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0004 | 0/0 | 5673 | 47 | 6 | 13 | 14 | 6 | 8 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0005 | 0/0 | 5673 | 22 | 3 | 2 | 15 | 1 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0006 | 0/0 | 5673 | 13 | 10 | 0 | 0 | 0 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0007 | 0/0 | 5673 | 10 | 10 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0008 | 0/0 | 5673 | 9 | 0 | 7 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0009 | 0/0 | 5673 | 8 | 0 | 0 | 8 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0010 | 0/1 | 5673 | 8 | 0 | 3 | 2 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0011 | 0/0 | 5673 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0012 | 0/0 | 5673 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0013 | 0/0 | 5673 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0014 | 0/0 | 5672 | 4 | 0 | 1 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0015 | 0/0 | 5673 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0016 | 0/0 | 5673 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0017 | 0/0 | 5673 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0018 | 0/0 | 5670 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0019 | 0/0 | 5673 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0020 | 0/0 | 5673 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0021 | 0/0 | 5672 | 2 | 0 | 0 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0022 | 0/0 | 5673 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0023 | 0/0 | 5673 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0024 | 0/0 | 5673 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0025 | 0/0 | 5673 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0026 | 0/0 | 5673 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0027 | 0/0 | 5673 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0028 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0029 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0030 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0031 | 0/0 | 5654 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0032 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0033 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0034 | 0/0 | 5672 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0035 | 0/0 | 5672 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0036 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0037 | 0/0 | 5671 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0038 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0039 | 0/0 | 5670 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0040 | 0/0 | 5670 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0041 | 0/0 | 5673 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0042 | 0/0 | 5732 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0043 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0044 | 1/0 | 5670 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0045 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0046 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0047 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0048 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0049 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0050 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0051 | 0/0 | 5671 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0052 | 0/0 | 5670 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0053 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0054 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0055 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0056 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0057 | 0/0 | 5671 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0058 | 0/0 | 5672 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0059 | 0/0 | 5671 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0060 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
t0061 | 0/0 | 5673 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
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 | 37 | 2 | 9 | 21 | 2 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0002 | 0/0 | 24 | 3 | 11 | 2 | 6 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0003 | 0/0 | 23 | 0 | 0 | 23 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0004 | 0/0 | 16 | 0 | 1 | 11 | 1 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0005 | 0/0 | 12 | 0 | 3 | 5 | 0 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0006 | 0/0 | 10 | 0 | 2 | 5 | 1 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0010 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0013 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0014 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0015 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0037 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
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 | 0/1 | 1287 | 177 | 38 | 34 | 79 | 8 | 17 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002 | 1/0 | 1287 | 101 | 11 | 17 | 54 | 4 | 14 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003 | 0/0 | 1287 | 101 | 22 | 7 | 61 | 2 | 9 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0005 | 0/0 | 1287 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0007 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0008 | 0/0 | 1287 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0009 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0011 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0002c0004 | 0/0 | 1287 | 11 | 11 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0003c0013 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0003c0014 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0004c0006 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0005c0010 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0006c0012 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6959 | 71 | 18 | 12 | 34 | 2 | 5 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0004 | 0/0 | 6959 | 47 | 6 | 13 | 14 | 6 | 8 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0008 | 0/0 | 6959 | 9 | 0 | 7 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0009 | 0/0 | 6959 | 8 | 0 | 0 | 8 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0010 | 0/1 | 6959 | 6 | 0 | 1 | 2 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0011 | 0/0 | 6959 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0012 | 0/0 | 6959 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0013 | 0/0 | 6959 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0016 | 0/0 | 6959 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0023 | 0/0 | 6959 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0027 | 0/0 | 6959 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0028 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0034 | 0/0 | 6958 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0035 | 0/0 | 6958 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0036 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0037 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0049 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0050 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0053 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0058 | 0/0 | 6958 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0059 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0060 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0001t0061 | 0/0 | 6959 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0002 | 0/0 | 6959 | 60 | 4 | 10 | 32 | 3 | 11 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0005 | 0/0 | 6959 | 22 | 3 | 2 | 15 | 1 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0015 | 0/0 | 6959 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0017 | 0/0 | 6959 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0020 | 0/0 | 6959 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0021 | 0/0 | 6958 | 2 | 0 | 0 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0025 | 0/0 | 6959 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0029 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0033 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0041 | 0/0 | 6959 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0042 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0043 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0002t0044 | 1/0 | 6956 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0001 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0003 | 0/0 | 6959 | 62 | 0 | 5 | 51 | 2 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0006 | 0/0 | 6959 | 10 | 7 | 0 | 0 | 0 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0014 | 0/0 | 6958 | 4 | 0 | 1 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0018 | 0/0 | 6956 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0019 | 0/0 | 6959 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0024 | 0/0 | 6959 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0026 | 0/0 | 6959 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0030 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0031 | 0/0 | 6940 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0032 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0038 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0039 | 0/0 | 6956 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0040 | 0/0 | 6956 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0045 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0046 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0047 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0051 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0052 | 0/0 | 6956 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0054 | 0/0 | 6959 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0055 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0056 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0003t0057 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0005t0002 | 0/0 | 6959 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0007t0006 | 0/0 | 6959 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0008t0010 | 0/0 | 6959 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0009t0001 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0001c0011t0006 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0002c0004t0007 | 0/0 | 6959 | 10 | 10 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0002c0004t0048 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0003c0013t0002 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0003c0014t0001 | 0/0 | 6959 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0004c0006t0022 | 0/0 | 6959 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0005c0010t0001 | 0/0 | 6959 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
a0006c0012t0002 | 0/0 | 6959 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | copy fasta | chr1 | 147637230 | 147675524 |
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 | 37 | 2 | 9 | 21 | 2 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0002 | 0/0 | 24 | 3 | 11 | 2 | 6 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0014 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0008g0015 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0009g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0010g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0010g0037 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0011g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0012g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0013g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0016g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0016g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0023g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0023g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0027g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0027g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0028g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0034g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0035g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0036g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0037g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0049g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0050g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0053g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0058g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0059g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0060g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0001t0061g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0005 | 0/0 | 12 | 0 | 3 | 5 | 0 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0006 | 0/0 | 10 | 0 | 2 | 5 | 1 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0013 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0015g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0017g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0020g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0021g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0021g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0025g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0029g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0033g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0041g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0042g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0043g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0002t0044g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0003 | 0/0 | 23 | 0 | 0 | 23 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0004 | 0/0 | 16 | 0 | 1 | 11 | 1 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0010 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0014g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0014g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0018g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0019g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0024g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0024g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0026g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0031g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0032g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0038g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0039g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0040g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0045g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0046g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0047g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0051g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0052g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0054g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0055g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0056g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0003t0057g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0005t0002g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0007t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0008t0010g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0008t0010g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0009t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0001c0011t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0002c0004t0007g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0002c0004t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0002c0004t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0002c0004t0048g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0003c0013t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0003c0014t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0004c0006t0022g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0005c0010t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
a0006c0012t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00099 | hp2 | a0001 | c0003 | t0003 | g0141 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00140 | hp1 | a0001 | c0002 | t0005 | g0013 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0004 | EUR | FIN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00408 | hp1 | a0001 | c0003 | t0056 | g0135 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00438 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00544 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00558 | hp2 | a0001 | c0001 | t0016 | g0181 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00597 | hp1 | a0001 | c0003 | t0024 | g0126 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00609 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00621 | hp2 | a0001 | c0003 | t0003 | g0124 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00673 | hp1 | a0001 | c0001 | t0060 | g0185 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00673 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00738 | hp1 | a0001 | c0001 | t0023 | g0144 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01069 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01069 | hp2 | a0001 | c0008 | t0010 | g0099 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01071 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01071 | hp2 | a0001 | c0008 | t0010 | g0119 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0036 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01081 | hp2 | a0001 | c0002 | t0005 | g0013 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01106 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01109 | hp1 | a0001 | c0005 | t0002 | g0039 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01168 | hp1 | a0001 | c0003 | t0014 | g0142 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01168 | hp2 | a0001 | c0002 | t0025 | g0042 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01169 | hp1 | a0001 | c0002 | t0025 | g0042 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01175 | hp2 | a0006 | c0012 | t0002 | g0116 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01192 | hp1 | a0001 | c0003 | t0003 | g0140 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0090 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0010 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0089 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0114 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01884 | hp2 | a0001 | c0003 | t0006 | g0021 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01891 | hp1 | a0001 | c0007 | t0006 | g0032 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01891 | hp2 | a0001 | c0003 | t0032 | g0048 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0133 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01978 | hp1 | a0001 | c0002 | t0005 | g0013 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01978 | hp2 | a0001 | c0003 | t0054 | g0138 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01981 | hp2 | a0001 | c0003 | t0003 | g0137 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02015 | hp1 | a0001 | c0001 | t0009 | g0072 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02040 | hp1 | a0001 | c0002 | t0043 | g0113 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02056 | hp2 | a0001 | c0001 | t0028 | g0047 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02074 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02083 | hp2 | a0001 | c0001 | t0037 | g0095 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02129 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02132 | hp2 | a0001 | c0003 | t0003 | g0123 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02135 | hp1 | a0001 | c0001 | t0036 | g0093 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02135 | hp2 | a0001 | c0002 | t0005 | g0177 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02145 | hp2 | a0004 | c0006 | t0022 | g0033 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02257 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02258 | hp1 | a0001 | c0003 | t0006 | g0021 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02280 | hp1 | a0001 | c0003 | t0006 | g0053 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02280 | hp2 | a0001 | c0003 | t0030 | g0050 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02572 | hp2 | a0002 | c0004 | t0007 | g0105 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02615 | hp2 | a0001 | c0002 | t0020 | g0040 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02622 | hp1 | a0001 | c0001 | t0059 | g0146 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02630 | hp1 | a0001 | c0003 | t0018 | g0046 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02630 | hp2 | a0001 | c0003 | t0006 | g0060 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02647 | hp2 | a0001 | c0003 | t0046 | g0102 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02717 | hp1 | a0001 | c0003 | t0006 | g0059 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02717 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02723 | hp1 | a0001 | c0003 | t0018 | g0046 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02723 | hp2 | a0001 | c0001 | t0049 | g0064 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02738 | hp1 | a0001 | c0001 | t0061 | g0186 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0037 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02809 | hp1 | a0001 | c0003 | t0006 | g0021 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02818 | hp1 | a0004 | c0006 | t0022 | g0033 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02895 | hp1 | a0001 | c0003 | t0026 | g0045 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02922 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02965 | hp2 | a0001 | c0001 | t0050 | g0175 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02970 | hp1 | a0001 | c0002 | t0033 | g0058 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0057 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02976 | hp1 | a0001 | c0001 | t0034 | g0049 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02976 | hp2 | a0001 | c0003 | t0039 | g0097 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03098 | hp1 | a0001 | c0003 | t0047 | g0063 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0122 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03130 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03139 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03139 | hp2 | a0001 | c0003 | t0006 | g0020 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0106 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03209 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03225 | hp1 | a0003 | c0014 | t0001 | g0162 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03225 | hp2 | a0001 | c0002 | t0029 | g0052 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0085 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03453 | hp1 | a0001 | c0003 | t0051 | g0148 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03486 | hp1 | a0001 | c0003 | t0018 | g0182 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03491 | hp1 | a0001 | c0002 | t0021 | g0079 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03579 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0109 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03669 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0101 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03710 | hp2 | a0001 | c0002 | t0041 | g0078 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03831 | hp2 | a0001 | c0003 | t0006 | g0020 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03834 | hp1 | a0001 | c0003 | t0006 | g0020 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03927 | hp2 | a0001 | c0003 | t0006 | g0051 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04184 | hp1 | a0001 | c0003 | t0019 | g0031 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0143 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18522 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18906 | hp2 | a0001 | c0003 | t0031 | g0055 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18940 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18940 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18942 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18942 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18944 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18945 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18946 | hp1 | a0001 | c0002 | t0015 | g0184 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18948 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18949 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18950 | hp2 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18951 | hp1 | a0001 | c0001 | t0035 | g0061 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18951 | hp2 | a0001 | c0003 | t0003 | g0129 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18956 | hp1 | a0001 | c0001 | t0010 | g0094 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18957 | hp1 | a0001 | c0003 | t0014 | g0134 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18957 | hp2 | a0001 | c0001 | t0058 | g0156 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18959 | hp2 | a0001 | c0003 | t0014 | g0136 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18962 | hp2 | a0005 | c0010 | t0001 | g0168 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18963 | hp1 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18963 | hp2 | a0001 | c0003 | t0003 | g0130 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18966 | hp1 | a0001 | c0003 | t0024 | g0128 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18968 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18968 | hp2 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18971 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18974 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18974 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18975 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18977 | hp1 | a0001 | c0003 | t0055 | g0127 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18978 | hp1 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18979 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18980 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18981 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18982 | hp1 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18982 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18983 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18984 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18985 | hp1 | a0001 | c0002 | t0005 | g0151 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18986 | hp2 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18988 | hp1 | a0001 | c0002 | t0005 | g0153 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18988 | hp2 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18989 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18989 | hp2 | a0001 | c0001 | t0027 | g0172 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18990 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18994 | hp2 | a0001 | c0002 | t0005 | g0152 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19001 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19004 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19005 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19007 | hp1 | a0001 | c0001 | t0027 | g0171 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19009 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19010 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19012 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19012 | hp2 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19043 | hp2 | a0001 | c0003 | t0052 | g0149 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19056 | hp1 | a0001 | c0003 | t0014 | g0139 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19056 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19058 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19059 | hp1 | a0001 | c0002 | t0021 | g0110 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19059 | hp2 | a0001 | c0003 | t0057 | g0132 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19060 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0155 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19062 | hp2 | a0001 | c0003 | t0038 | g0100 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19063 | hp1 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19063 | hp2 | a0001 | c0002 | t0005 | g0154 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19065 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0036 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19070 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19072 | hp1 | a0001 | c0002 | t0042 | g0084 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19072 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19074 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19074 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19078 | hp1 | a0001 | c0001 | t0053 | g0158 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19078 | hp2 | a0001 | c0003 | t0003 | g0125 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19079 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19079 | hp2 | a0001 | c0001 | t0023 | g0180 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19080 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19081 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19084 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19088 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19090 | hp1 | a0003 | c0013 | t0002 | g0083 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19240 | hp1 | a0002 | c0004 | t0048 | g0103 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA19240 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20129 | hp1 | a0001 | c0005 | t0002 | g0039 | AFR | ASW | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | ASW | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0041 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20905 | hp1 | a0001 | c0002 | t0005 | g0178 | SAS | GIH | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA20905 | hp2 | a0001 | c0003 | t0019 | g0031 | SAS | GIH | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02109 | hp2 | a0002 | c0004 | t0007 | g0104 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02486 | hp1 | a0001 | c0007 | t0006 | g0032 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02486 | hp2 | a0001 | c0003 | t0045 | g0062 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG02559 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03471 | hp1 | a0001 | c0003 | t0026 | g0045 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG06807 | hp1 | a0001 | c0002 | t0020 | g0040 | AFR | USA | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
HG06807 | hp2 | a0001 | c0011 | t0006 | g0054 | AFR | USA | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA21309 | hp1 | a0001 | c0003 | t0040 | g0096 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0037 | REF | REF | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0044 | g0065 | REF | REF | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:147647506
|
T | C | 1 | a0004 | 2 | HG02145.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.1204A>G | p.Met402Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1680/6956 | 1204/1287 | 402/428 | chr1 | 147647506 | ||
chr1:147648394
|
G | A | 1 | a0004 | 2 | HG02145.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.995C>T | p.Ala332Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/10 | 1471/6956 | 995/1287 | 332/428 | chr1 | 147648394 | ||
chr1:147650174
|
T | C | 1 | a0002 | 11 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.946A>G | p.Met316Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1422/6956 | 946/1287 | 316/428 | chr1 | 147650174 | ||
chr1:147650194
|
T | C | 1 | a0005 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.926A>G | p.Glu309Gly | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1402/6956 | 926/1287 | 309/428 | chr1 | 147650194 | ||
chr1:147650195
|
C | T | 1 | a0005 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.925G>A | p.Glu309Lys | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1401/6956 | 925/1287 | 309/428 | chr1 | 147650195 | ||
chr1:147654322
|
G | A | 1 | a0006 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.652C>T | p.Arg218Trp | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/10 | 1128/6956 | 652/1287 | 218/428 | chr1 | 147654322 | ||
chr1:147659696
|
G | A | 1 | a0003 | 2 | HG03225.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.299C>T | p.Pro100Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/10 | 775/6956 | 299/1287 | 100/428 | chr1 | 147659696 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:147647471
|
G | A | 5 | a0001c0001a0001c0008a0001c0009others(2): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
synonymous_variant | LOW | c.1239C>T | p.His413His | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1715/6956 | 1239/1287 | 413/428 | chr1 | 147647471 | ||
chr1:147648369
|
C | A | 1 | a0001c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1020G>T | p.Pro340Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/10 | 1496/6956 | 1020/1287 | 340/428 | chr1 | 147648369 | ||
chr1:147652507
|
T | G | 9 | a0001c0001a0001c0003a0001c0007others(6): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
synonymous_variant | LOW | c.823A>C | p.Arg275Arg | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/10 | 1299/6956 | 823/1287 | 275/428 | chr1 | 147652507 | ||
chr1:147654302
|
T | C | 1 | a0001c0007 | 2 | HG01891.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.672A>G | p.Leu224Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/10 | 1148/6956 | 672/1287 | 224/428 | chr1 | 147654302 | ||
chr1:147658988
|
C | T | 1 | a0001c0005 | 2 | HG01109.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.531G>A | p.Leu177Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/10 | 1007/6956 | 531/1287 | 177/428 | chr1 | 147658988 | ||
chr1:147659689
|
T | C | 1 | a0001c0008 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.306A>G | p.Pro102Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/10 | 782/6956 | 306/1287 | 102/428 | chr1 | 147659689 | ||
chr1:147669857
|
A | G | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.192T>C | p.Pro64Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 668/6956 | 192/1287 | 64/428 | chr1 | 147669857 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:147642386
|
T | C | 1 | a0001c0003t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5037A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 5037 | chr1 | 147642386 | |||||
chr1:147642394
|
C | G | 1 | a0001c0002t0025 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5029G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 5029 | chr1 | 147642394 | |||||
chr1:147642472
|
T | G | 2 | a0001c0003t0039a0001c0003t0040 | 2 | HG02976.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4951A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4951 | chr1 | 147642472 | |||||
chr1:147642474
|
T | C | 1 | a0001c0001t0058 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4949A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4949 | chr1 | 147642474 | |||||
chr1:147642476
|
C | CT | 15 | a0001c0001t0008a0001c0001t0027a0001c0002t0002others(12): Show | 110 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4946dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4946 | chr1 | 147642476 | |||||
chr1:147642476
|
C | T | 1 | a0001c0001t0058 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4947G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4947 | chr1 | 147642476 | |||||
chr1:147642485
|
T | A | 1 | a0001c0001t0058 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4938A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4938 | chr1 | 147642485 | |||||
chr1:147642485
|
T | TA | 53 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(50): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*4937dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4937 | chr1 | 147642485 | |||||
chr1:147642503
|
G | A | 27 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(24): Show | 175 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*4920C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4920 | chr1 | 147642503 | |||||
chr1:147642814
|
C | T | 1 | a0001c0001t0036 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4609G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4609 | chr1 | 147642814 | |||||
chr1:147642918
|
GAAA | G | 3 | a0001c0003t0018a0001c0003t0039a0001c0003t0040 | 5 | HG02630.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4502_*4504delTTT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4502 | chr1 | 147642918 | |||||
chr1:147642925
|
A | G | 1 | a0002c0004t0048 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4498T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4498 | chr1 | 147642925 | |||||
chr1:147643010
|
C | T | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4413G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4413 | chr1 | 147643010 | |||||
chr1:147643320
|
G | A | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4103C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4103 | chr1 | 147643320 | |||||
chr1:147643425
|
A | C | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3998 | chr1 | 147643425 | |||||
chr1:147643601
|
A | G | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3822T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3822 | chr1 | 147643601 | |||||
chr1:147643626
|
C | T | 1 | a0001c0003t0054 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3797G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3797 | chr1 | 147643626 | |||||
chr1:147643632
|
T | G | 9 | a0001c0003t0006a0001c0003t0026a0001c0003t0031others(6): Show | 20 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3791A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3791 | chr1 | 147643632 | |||||
chr1:147643722
|
T | C | 1 | a0001c0002t0043 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3701A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3701 | chr1 | 147643722 | |||||
chr1:147643819
|
A | T | 10 | a0001c0003t0006a0001c0003t0026a0001c0003t0030others(7): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3604T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3604 | chr1 | 147643819 | |||||
chr1:147644356
|
G | A | 1 | a0001c0002t0015 | 4 | NA18946.hp1 NA18963.hp1 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3067C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3067 | chr1 | 147644356 | |||||
chr1:147644394
|
G | A | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3029C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3029 | chr1 | 147644394 | |||||
chr1:147644466
|
G | A | 1 | a0001c0003t0039 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2957C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2957 | chr1 | 147644466 | |||||
chr1:147644493
|
T | C | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2930A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2930 | chr1 | 147644493 | |||||
chr1:147644548
|
C | T | 1 | a0001c0003t0039 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2875G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2875 | chr1 | 147644548 | |||||
chr1:147644569
|
G | GGTAAAAG others(52): Show |
1 | a0001c0002t0042 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795_*2853dupAATT others(55): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2853 | chr1 | 147644569 | |||||
chr1:147644592
|
A | C | 1 | a0001c0002t0041 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2831T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2831 | chr1 | 147644592 | |||||
chr1:147644602
|
A | G | 10 | a0001c0003t0006a0001c0003t0026a0001c0003t0031others(7): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2821T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2821 | chr1 | 147644602 | |||||
chr1:147644647
|
G | A | 1 | a0001c0003t0056 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2776C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2776 | chr1 | 147644647 | |||||
chr1:147644677
|
A | G | 1 | a0001c0003t0045 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2746T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2746 | chr1 | 147644677 | |||||
chr1:147644716
|
C | T | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0028others(1): Show | 14 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2707G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2707 | chr1 | 147644716 | |||||
chr1:147644792
|
G | A | 3 | a0001c0003t0024a0001c0003t0039a0001c0003t0040 | 4 | HG00597.hp1 HG02976.hp2 NA18966.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2631C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2631 | chr1 | 147644792 | |||||
chr1:147644805
|
C | T | 3 | a0001c0003t0018a0001c0003t0039a0001c0003t0040 | 5 | HG02630.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2618G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2618 | chr1 | 147644805 | |||||
chr1:147644981
|
C | CT | 4 | a0001c0001t0034a0001c0001t0035a0001c0002t0021others(1): Show | 8 | HG01168.hp1 HG02976.hp1 HG03491.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2441dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2441 | chr1 | 147644981 | |||||
chr1:147644981
|
C | CTT | 61 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(58): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
3_prime_UTR_variant | MODIFIER | c.*2440_*2441dupAA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2441 | chr1 | 147644981 | |||||
chr1:147645193
|
A | C | 1 | a0004c0006t0022 | 2 | HG02145.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2230T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2230 | chr1 | 147645193 | |||||
chr1:147645194
|
ATATAATA others(12): Show |
A | 1 | a0001c0003t0031 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2210_*2228delATTT others(15): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2210 | chr1 | 147645194 | |||||
chr1:147645423
|
G | A | 1 | a0001c0003t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2000 | chr1 | 147645423 | |||||
chr1:147645486
|
C | T | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1937 | chr1 | 147645486 | |||||
chr1:147645738
|
T | C | 13 | a0001c0003t0006a0001c0003t0026a0001c0003t0030others(10): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1685A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1685 | chr1 | 147645738 | |||||
chr1:147645935
|
T | G | 1 | a0001c0001t0013 | 4 | HG02109.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1488A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1488 | chr1 | 147645935 | |||||
chr1:147646084
|
G | A | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1339C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1339 | chr1 | 147646084 | |||||
chr1:147646147
|
T | A | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1276A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1276 | chr1 | 147646147 | |||||
chr1:147646204
|
T | C | 11 | a0001c0003t0006a0001c0003t0026a0001c0003t0030others(8): Show | 22 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1219A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1219 | chr1 | 147646204 | |||||
chr1:147646264
|
G | A | 1 | a0001c0003t0019 | 2 | HG04184.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1159C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1159 | chr1 | 147646264 | |||||
chr1:147646283
|
A | G | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1140T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1140 | chr1 | 147646283 | |||||
chr1:147646326
|
G | A | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1097C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1097 | chr1 | 147646326 | |||||
chr1:147646379
|
T | C | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(29): Show | 197 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1044A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1044 | chr1 | 147646379 | |||||
chr1:147646668
|
C | T | 9 | a0001c0003t0003a0001c0003t0014a0001c0003t0019others(6): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*755G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 755 | chr1 | 147646668 | |||||
chr1:147646698
|
A | G | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0023others(3): Show | 61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 725 | chr1 | 147646698 | |||||
chr1:147646804
|
C | T | 1 | a0001c0001t0012 | 6 | NA18940.hp2 NA18971.hp2 NA18974.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*619G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 619 | chr1 | 147646804 | |||||
chr1:147646818
|
A | G | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*605T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 605 | chr1 | 147646818 | |||||
chr1:147646899
|
G | A | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*524C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 524 | chr1 | 147646899 | |||||
chr1:147646988
|
G | C | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*435C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 435 | chr1 | 147646988 | |||||
chr1:147647125
|
T | C | 1 | a0001c0001t0053 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 298 | chr1 | 147647125 | |||||
chr1:147647126
|
A | T | 1 | a0001c0001t0053 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 297 | chr1 | 147647126 | |||||
chr1:147647308
|
A | C | 2 | a0001c0003t0051a0001c0003t0052 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 115 | chr1 | 147647308 | |||||
chr1:147647321
|
A | G | 1 | a0001c0001t0050 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 102 | chr1 | 147647321 | |||||
chr1:147647375
|
T | A | 1 | a0001c0001t0049 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 48 | chr1 | 147647375 | |||||
chr1:147670155
|
G | C | 1 | a0001c0001t0060 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 107 | chr1 | 147670155 | |||||
chr1:147670174
|
T | C | 40 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(37): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(226): Show |
5_prime_UTR_variant | MODIFIER | c.-126A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 126 | chr1 | 147670174 | |||||
chr1:147670230
|
C | G | 1 | a0001c0001t0035 | 1 | NA18951.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 182 | chr1 | 147670230 | |||||
chr1:147670231
|
G | A | 1 | a0001c0001t0061 | 1 | HG02738.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-183C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | chr1 | 147670231 | ||||||
chr1:147670335
|
C | T | 10 | a0001c0001t0011a0001c0001t0034a0001c0002t0029others(7): Show | 25 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-287G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 287 | chr1 | 147670335 | |||||
chr1:147670473
|
A | G | 1 | a0001c0003t0019 | 2 | HG04184.hp1 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-425T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 425 | chr1 | 147670473 | |||||
chr1:147670485
|
C | T | 1 | a0001c0001t0028 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-437G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 437 | chr1 | 147670485 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:147647595
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1144-29G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647595 | ||||||
chr1:147647599
|
G | A | 1 | a0001c0003t0003g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1144-33C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647599 | ||||||
chr1:147647835
|
G | A | 3 | a0001c0003t0003g0010a0001c0003t0014g0139a0001c0003t0054g0138 | 9 | HG01346.hp1 HG01978.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-269C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647835 | ||||||
chr1:147647982
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 10 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+264G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647982 | ||||||
chr1:147648029
|
G | C | 1 | a0005c0010t0001g0168 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1143+217C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147648029 | ||||||
chr1:147648126
|
G | A | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1143+120C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147648126 | ||||||
chr1:147648446
|
C | G | 1 | a0001c0002t0005g0153 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.978-35G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147648446 | ||||||
chr1:147648616
|
C | T | 1 | a0001c0001t0004g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.978-205G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147648616 | ||||||
chr1:147649175
|
C | T | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-764G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649175 | ||||||
chr1:147649198
|
G | A | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-787C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649198 | ||||||
chr1:147649213
|
C | T | 2 | a0001c0002t0002g0071a0001c0002t0002g0077 | 2 | NA18960.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.978-802G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649213 | ||||||
chr1:147649246
|
G | A | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-835C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649246 | ||||||
chr1:147649276
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-865A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649276 | ||||||
chr1:147649431
|
G | C | 1 | a0001c0002t0042g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.977+712C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649431 | ||||||
chr1:147649432
|
C | G | 1 | a0001c0002t0042g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.977+711G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649432 | ||||||
chr1:147649451
|
A | AT | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(178): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.977+691dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649451 | ||||||
chr1:147649451
|
A | ATT | 4 | a0001c0003t0006g0021a0001c0003t0006g0059a0001c0003t0051g0148others(1): Show | 6 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.977+690_977+691dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649451 | ||||||
chr1:147649828
|
A | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977+315T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649828 | ||||||
chr1:147649941
|
A | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977+202T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649941 | ||||||
chr1:147650007
|
A | C | 1 | a0001c0002t0002g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.977+136T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147650007 | ||||||
chr1:147650009
|
T | C | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.977+134A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147650009 | ||||||
chr1:147650422
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-184A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650422 | ||||||
chr1:147650667
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-429A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650667 | ||||||
chr1:147650704
|
A | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-466T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650704 | ||||||
chr1:147650813
|
T | C | 29 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(26): Show | 65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.882-575A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650813 | ||||||
chr1:147650889
|
G | T | 1 | a0001c0003t0006g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.882-651C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650889 | ||||||
chr1:147650973
|
T | C | 1 | a0001c0003t0003g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.882-735A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650973 | ||||||
chr1:147651028
|
C | T | 29 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(26): Show | 65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.882-790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651028 | ||||||
chr1:147651286
|
T | C | 1 | a0001c0002t0002g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-1048A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651286 | ||||||
chr1:147651311
|
T | C | 1 | a0001c0002t0005g0154 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.882-1073A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651311 | ||||||
chr1:147651339
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-1101A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651339 | ||||||
chr1:147651367
|
C | T | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+1082G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651367 | ||||||
chr1:147651387
|
C | A | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+1062G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651387 | ||||||
chr1:147651435
|
G | A | 15 | a0001c0003t0006g0020a0001c0003t0006g0021a0001c0003t0006g0051others(12): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.881+1014C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651435 | ||||||
chr1:147651537
|
C | T | 3 | a0001c0001t0013g0024a0001c0001t0013g0106a0004c0006t0022g0033 | 6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+912G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651537 | ||||||
chr1:147651616
|
G | T | 3 | a0001c0001t0013g0024a0001c0001t0013g0106a0004c0006t0022g0033 | 6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+833C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651616 | ||||||
chr1:147651639
|
C | T | 1 | a0001c0001t0013g0024 | 3 | HG02109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.881+810G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651639 | ||||||
chr1:147651671
|
C | T | 1 | a0001c0003t0051g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+778G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651671 | ||||||
chr1:147651733
|
G | A | 1 | a0001c0001t0027g0172 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.881+716C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651733 | ||||||
chr1:147651831
|
C | T | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+618G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651831 | ||||||
chr1:147652080
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.881+369G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652080 | ||||||
chr1:147652223
|
G | A | 1 | a0001c0003t0039g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.881+226C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652223 | ||||||
chr1:147652232
|
T | C | 1 | a0002c0004t0007g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.881+217A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652232 | ||||||
chr1:147652589
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-40A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652589 | ||||||
chr1:147652753
|
G | GAA | 29 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(26): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.781-206_781-205dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652753 | ||||||
chr1:147652753
|
G | GAAA | 148 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(145): Show | 319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.781-207_781-205dup others(3): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652753 | ||||||
chr1:147652753
|
G | GAAAA | 7 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0004g0086others(4): Show | 8 | HG00673.hp2 HG01952.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-208_781-205dup others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652753 | ||||||
chr1:147652837
|
G | GT | 174 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(171): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.781-289dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652837 | ||||||
chr1:147652837
|
G | GTT | 7 | a0001c0001t0001g0167a0001c0001t0053g0158a0001c0002t0002g0073others(4): Show | 7 | HG00408.hp2 HG00597.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-290_781-289dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652837 | ||||||
chr1:147652837
|
G | T | 3 | a0001c0001t0004g0069a0001c0002t0002g0112a0001c0002t0005g0152 | 3 | HG00735.hp2 NA18949.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.781-288C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652837 | ||||||
chr1:147652858
|
G | A | 1 | a0001c0002t0002g0025 | 3 | HG01243.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.781-309C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652858 | ||||||
chr1:147652889
|
C | CGATCTCG others(299): Show |
2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | ||||||
chr1:147652889
|
C | CGATCTCG others(299): Show |
1 | a0001c0001t0004g0070 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | ||||||
chr1:147652889
|
C | CGATCTCG others(299): Show |
6 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0001t0034g0049others(3): Show | 9 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | ||||||
chr1:147652889
|
C | CGATCTCG others(300): Show |
51 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(48): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.781-341_781-340ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | ||||||
chr1:147652895
|
C | CGGCTCAC others(299): Show |
1 | a0001c0001t0049g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781-347_781-346ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652895 | ||||||
chr1:147652896
|
G | A | 1 | a0001c0002t0002g0108 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.781-347C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652896 | ||||||
chr1:147652919
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(126): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.781-370A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | ||||||
chr1:147652919
|
T | TGGGTTCA others(299): Show |
1 | a0001c0002t0002g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.781-371_781-370ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | ||||||
chr1:147652919
|
T | TGGGTTCA others(299): Show |
43 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0019others(40): Show | 93 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.781-371_781-370ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | ||||||
chr1:147652919
|
T | TGGGTTCA others(300): Show |
1 | a0001c0002t0005g0155 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.781-371_781-370ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | ||||||
chr1:147652922
|
G | GTTCACGC others(300): Show |
1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.781-374_781-373ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652922 | ||||||
chr1:147652922
|
G | GTTCACGC others(299): Show |
5 | a0001c0002t0033g0058a0002c0004t0007g0008a0002c0004t0007g0104others(2): Show | 12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.781-374_781-373ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652922 | ||||||
chr1:147652927
|
C | CGCCATTT others(299): Show |
14 | a0001c0003t0006g0020a0001c0003t0006g0021a0001c0003t0006g0051others(11): Show | 20 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.781-379_781-378ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652927 | ||||||
chr1:147652955
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.781-406A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652955 | ||||||
chr1:147652970
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-421C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652970 | ||||||
chr1:147652987
|
C | CGGCTAAT others(299): Show |
1 | a0001c0003t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.781-439_781-438ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652987 | ||||||
chr1:147652993
|
A | ATTTTTTT others(300): Show |
1 | a0001c0001t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.781-445_781-444ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652993 | ||||||
chr1:147653018
|
G | AGGGTTTC others(299): Show |
4 | a0001c0002t0002g0023a0001c0002t0002g0074a0001c0002t0042g0084others(1): Show | 6 | NA18955.hp2 NA18999.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-469_781-468ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653018 | ||||||
chr1:147653083
|
T | TCCCAAAT others(301): Show |
1 | a0001c0003t0003g0125 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.781-535_781-534ins others(308): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653083 | ||||||
chr1:147653119
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0176others(1): Show | 4 | HG02965.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-570C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | ||||||
chr1:147653119
|
G | GCCTGGCC others(299): Show |
43 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(40): Show | 110 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.781-571_781-570ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | ||||||
chr1:147653119
|
G | GCCTGGCC others(300): Show |
1 | a0001c0001t0001g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.781-571_781-570ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | ||||||
chr1:147653122
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(127): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.781-573G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653122 | ||||||
chr1:147653135
|
T | TGTTTTTT others(300): Show |
2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-587_781-586ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653135 | ||||||
chr1:147653137
|
G | GTTTTTTT others(300): Show |
1 | a0001c0002t0002g0075 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.781-589_781-588ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | ||||||
chr1:147653137
|
G | GTTTTTTT others(300): Show |
1 | a0001c0001t0053g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.781-589_781-588ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | ||||||
chr1:147653137
|
G | T | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-588C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | ||||||
chr1:147653200
|
G | A | 1 | a0001c0003t0030g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-651C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653200 | ||||||
chr1:147653209
|
C | G | 1 | a0003c0014t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-660G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653209 | ||||||
chr1:147653290
|
C | A | 5 | a0001c0002t0033g0058a0002c0004t0007g0008a0002c0004t0007g0104others(2): Show | 12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.781-741G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653290 | ||||||
chr1:147653385
|
T | C | 42 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(39): Show | 84 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.780+809A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653385 | ||||||
chr1:147653415
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.780+779G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653415 | ||||||
chr1:147653443
|
T | TAA | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(178): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.780+749_780+750dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653443 | ||||||
chr1:147653535
|
A | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.780+659T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653535 | ||||||
chr1:147654126
|
A | C | 1 | a0001c0003t0003g0125 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.780+68T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147654126 | ||||||
chr1:147654437
|
AT | A | 3 | a0001c0001t0013g0024a0001c0001t0013g0106a0004c0006t0022g0033 | 6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-112delA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654437 | ||||||
chr1:147654531
|
G | A | 1 | a0001c0001t0016g0181 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.648-205C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654531 | ||||||
chr1:147654600
|
G | C | 1 | a0001c0002t0005g0155 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.648-274C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654600 | ||||||
chr1:147654827
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.647+334A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654827 | ||||||
chr1:147654907
|
G | A | 1 | a0001c0001t0008g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.647+254C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654907 | ||||||
chr1:147654954
|
T | C | 1 | a0001c0003t0003g0129 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.647+207A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654954 | ||||||
chr1:147655014
|
G | A | 17 | a0001c0001t0034g0049a0001c0002t0029g0052a0001c0002t0033g0058others(14): Show | 23 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.647+147C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147655014 | ||||||
chr1:147655487
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(45): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.560-239C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655487 | ||||||
chr1:147655616
|
T | G | 37 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0001t0049g0064others(34): Show | 87 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.560-368A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655616 | ||||||
chr1:147655622
|
T | C | 31 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(28): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.560-374A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655622 | ||||||
chr1:147655689
|
C | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.560-441G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655689 | ||||||
chr1:147655844
|
T | A | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.560-596A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655844 | ||||||
chr1:147655882
|
G | A | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.560-634C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655882 | ||||||
chr1:147656034
|
T | C | 1 | a0001c0002t0017g0026 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.560-786A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656034 | ||||||
chr1:147656493
|
A | C | 29 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(26): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.560-1245T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656493 | ||||||
chr1:147656613
|
T | C | 2 | a0001c0003t0003g0141a0001c0003t0014g0142 | 2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.560-1365A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656613 | ||||||
chr1:147656893
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.560-1645A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656893 | ||||||
chr1:147656896
|
A | G | 1 | a0003c0014t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.560-1648T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656896 | ||||||
chr1:147656899
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(132): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.560-1651C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656899 | ||||||
chr1:147656921
|
T | C | 1 | a0001c0001t0049g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560-1673A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656921 | ||||||
chr1:147657037
|
C | A | 1 | a0001c0001t0010g0094 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.560-1789G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657037 | ||||||
chr1:147657040
|
C | G | 1 | a0001c0002t0002g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.560-1792G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657040 | ||||||
chr1:147657148
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.559+1812T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657148 | ||||||
chr1:147657208
|
C | CCA | 29 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(26): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.559+1750_559+1751d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657208 | ||||||
chr1:147657274
|
G | A | 4 | a0001c0002t0033g0058a0001c0003t0006g0021a0001c0003t0006g0059others(1): Show | 6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+1686C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657274 | ||||||
chr1:147657461
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0009t0001g0122 | 7 | HG01175.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.559+1499G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657461 | ||||||
chr1:147657466
|
G | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(46): Show | 116 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.559+1494C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657466 | ||||||
chr1:147657506
|
C | T | 1 | a0001c0001t0008g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.559+1454G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657506 | ||||||
chr1:147657514
|
G | A | 1 | a0001c0002t0002g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.559+1446C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657514 | ||||||
chr1:147657605
|
C | G | 31 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0003t0003g0003others(28): Show | 79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.559+1355G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657605 | ||||||
chr1:147657612
|
G | T | 31 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0003t0003g0003others(28): Show | 79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.559+1348C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657612 | ||||||
chr1:147657671
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(131): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.559+1289T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657671 | ||||||
chr1:147657885
|
T | C | 68 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(65): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.559+1075A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657885 | ||||||
chr1:147657893
|
G | A | 1 | a0001c0002t0002g0041 | 2 | HG00639.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.559+1067C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657893 | ||||||
chr1:147657928
|
T | C | 28 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(25): Show | 65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.559+1032A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657928 | ||||||
chr1:147658107
|
T | C | 30 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0003t0003g0003others(27): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.559+853A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658107 | ||||||
chr1:147658160
|
A | G | 67 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(64): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.559+800T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658160 | ||||||
chr1:147658170
|
C | T | 6 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0073others(3): Show | 10 | HG00408.hp2 HG02015.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658170 | ||||||
chr1:147658240
|
T | C | 37 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(34): Show | 82 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.559+720A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658240 | ||||||
chr1:147658410
|
C | T | 1 | a0001c0003t0014g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.559+550G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658410 | ||||||
chr1:147658461
|
T | A | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.559+499A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658461 | ||||||
chr1:147658465
|
G | A | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.559+495C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658465 | ||||||
chr1:147658477
|
G | A | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.559+483C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658477 | ||||||
chr1:147658546
|
C | T | 22 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(19): Show | 58 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.559+414G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658546 | ||||||
chr1:147658650
|
G | A | 1 | a0001c0002t0002g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.559+310C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658650 | ||||||
chr1:147658655
|
C | T | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.559+305G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658655 | ||||||
chr1:147658660
|
T | C | 1 | a0001c0002t0002g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.559+300A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658660 | ||||||
chr1:147659207
|
G | T | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.480-168C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659207 | ||||||
chr1:147659208
|
A | T | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.480-169T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659208 | ||||||
chr1:147659214
|
A | G | 1 | a0001c0003t0003g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.480-175T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659214 | ||||||
chr1:147659235
|
C | T | 2 | a0001c0001t0013g0024a0001c0001t0013g0106 | 4 | HG02109.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+161G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659235 | ||||||
chr1:147659350
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(123): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.479+46A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659350 | ||||||
chr1:147659386
|
A | T | 36 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(33): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.479+10T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659386 | ||||||
chr1:147659547
|
AAAG | A | 17 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0034g0049others(14): Show | 26 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.349-24_349-22delCT others(1): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659547 | ||||||
chr1:147659595
|
A | C | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.348+52T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659595 | ||||||
chr1:147659605
|
C | A | 1 | a0001c0001t0008g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.348+42G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659605 | ||||||
chr1:147659642
|
C | T | 1 | a0001c0001t0001g0044 | 2 | NA18945.hp2 NA18953.hp1 |
splice_region_variant&intron_variant | LOW | c.348+5G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659642 | ||||||
chr1:147659830
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(123): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.220-55A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147659830 | ||||||
chr1:147659890
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.220-115T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147659890 | ||||||
chr1:147660017
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.220-242C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660017 | ||||||
chr1:147660086
|
G | A | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-311C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660086 | ||||||
chr1:147660169
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220-394A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660169 | ||||||
chr1:147660176
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220-401C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660176 | ||||||
chr1:147660250
|
C | T | 1 | a0001c0003t0006g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220-475G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660250 | ||||||
chr1:147660300
|
C | A | 1 | a0001c0002t0002g0117 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.220-525G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660300 | ||||||
chr1:147660620
|
A | G | 3 | a0001c0001t0049g0064a0001c0003t0045g0062a0001c0003t0047g0063 | 3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.220-845T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660620 | ||||||
chr1:147660625
|
C | T | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-850G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660625 | ||||||
chr1:147660710
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-935A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660710 | ||||||
chr1:147660963
|
T | C | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-1188A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660963 | ||||||
chr1:147661127
|
T | C | 1 | a0001c0002t0005g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-1352A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661127 | ||||||
chr1:147661164
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(39): Show | 105 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.220-1389C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661164 | ||||||
chr1:147661273
|
C | T | 1 | a0001c0003t0051g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-1498G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661273 | ||||||
chr1:147661315
|
A | AT | 116 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0043others(113): Show | 242 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.220-1541dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661315 | ||||||
chr1:147661315
|
A | ATT | 33 | a0001c0001t0001g0011a0001c0001t0001g0159a0001c0001t0001g0160others(30): Show | 84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.220-1542_220-1541d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661315 | ||||||
chr1:147661337
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(42): Show | 108 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.220-1562C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661337 | ||||||
chr1:147661474
|
C | T | 1 | a0001c0002t0002g0111 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.220-1699G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661474 | ||||||
chr1:147661492
|
C | T | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-1717G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661492 | ||||||
chr1:147661513
|
T | C | 17 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0034g0049others(14): Show | 26 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.220-1738A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661513 | ||||||
chr1:147661589
|
T | A | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-1814A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661589 | ||||||
chr1:147661591
|
A | T | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-1816T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661591 | ||||||
chr1:147661668
|
A | G | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-1893T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661668 | ||||||
chr1:147661678
|
G | A | 1 | a0002c0004t0007g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.220-1903C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661678 | ||||||
chr1:147661788
|
A | C | 1 | a0001c0001t0004g0088 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.220-2013T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661788 | ||||||
chr1:147661981
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.220-2206A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661981 | ||||||
chr1:147662044
|
T | C | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-2269A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662044 | ||||||
chr1:147662283
|
A | AT | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-2509dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662283 | ||||||
chr1:147662672
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0050g0175 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.220-2897A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662672 | ||||||
chr1:147662687
|
T | C | 18 | a0001c0001t0010g0085a0001c0001t0011g0018a0001c0001t0011g0056others(15): Show | 27 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.220-2912A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662687 | ||||||
chr1:147662710
|
C | T | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-2935G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662710 | ||||||
chr1:147662944
|
A | T | 1 | a0001c0002t0021g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-3169T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662944 | ||||||
chr1:147662956
|
T | A | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-3181A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662956 | ||||||
chr1:147663121
|
A | G | 1 | a0001c0001t0004g0087 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.220-3346T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663121 | ||||||
chr1:147663195
|
C | T | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-3420G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663195 | ||||||
chr1:147663226
|
G | C | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3451C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663226 | ||||||
chr1:147663290
|
G | GC | 130 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(127): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.220-3516_220-3515i others(3): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663290 | ||||||
chr1:147663291
|
T | C | 1 | a0001c0003t0057g0132 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220-3516A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663291 | ||||||
chr1:147663292
|
G | T | 1 | a0001c0003t0057g0132 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220-3517C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663292 | ||||||
chr1:147663355
|
A | G | 2 | a0001c0003t0051g0148a0001c0003t0052g0149 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-3580T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663355 | ||||||
chr1:147663473
|
A | G | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3698T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663473 | ||||||
chr1:147663515
|
A | G | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3740T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663515 | ||||||
chr1:147663587
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(39): Show | 102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.220-3812G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663587 | ||||||
chr1:147663649
|
A | G | 1 | a0001c0003t0047g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.220-3874T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663649 | ||||||
chr1:147663658
|
A | T | 1 | a0001c0002t0002g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.220-3883T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663658 | ||||||
chr1:147663733
|
A | C | 28 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0010others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3958T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663733 | ||||||
chr1:147663749
|
T | C | 1 | a0001c0003t0003g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220-3974A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663749 | ||||||
chr1:147663916
|
C | CA | 185 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(182): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.220-4142dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663916 | ||||||
chr1:147664166
|
G | A | 32 | a0001c0001t0004g0002a0001c0001t0004g0035a0001c0001t0004g0067others(29): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.220-4391C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664166 | ||||||
chr1:147664206
|
C | T | 1 | a0001c0001t0011g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.220-4431G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664206 | ||||||
chr1:147664277
|
C | T | 1 | a0001c0003t0032g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.220-4502G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664277 | ||||||
chr1:147664384
|
A | G | 16 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0034g0049others(13): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.220-4609T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664384 | ||||||
chr1:147664455
|
T | C | 46 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0016g0181others(43): Show | 100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.220-4680A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664455 | ||||||
chr1:147664515
|
G | C | 1 | a0001c0003t0038g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220-4740C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664515 | ||||||
chr1:147664654
|
A | G | 16 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0034g0049others(13): Show | 24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.220-4879T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664654 | ||||||
chr1:147664733
|
G | A | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-4958C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664733 | ||||||
chr1:147664806
|
A | G | 1 | a0001c0003t0030g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.219+5024T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664806 | ||||||
chr1:147664983
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219+4847G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664983 | ||||||
chr1:147665106
|
T | C | 45 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0011g0057others(42): Show | 99 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.219+4724A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665106 | ||||||
chr1:147665250
|
T | C | 45 | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0011g0057others(42): Show | 99 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.219+4580A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665250 | ||||||
chr1:147665557
|
C | T | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219+4273G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665557 | ||||||
chr1:147665695
|
G | A | 1 | a0001c0002t0002g0019 | 4 | HG02145.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4135C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665695 | ||||||
chr1:147665765
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0058g0156 | 3 | HG02074.hp2 HG02132.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.219+4065T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665765 | ||||||
chr1:147665784
|
G | A | 5 | a0001c0003t0046g0102a0002c0004t0007g0008a0002c0004t0007g0104others(2): Show | 12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.219+4046C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665784 | ||||||
chr1:147665846
|
A | G | 1 | a0001c0001t0058g0156 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.219+3984T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665846 | ||||||
chr1:147665867
|
C | T | 28 | a0001c0001t0023g0144a0001c0003t0003g0003a0001c0003t0003g0004others(25): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.219+3963G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665867 | ||||||
chr1:147665916
|
A | C | 7 | a0001c0002t0002g0071a0001c0002t0005g0007a0001c0002t0005g0151others(4): Show | 15 | HG00438.hp1 HG02129.hp2 NA18974.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+3914T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665916 | ||||||
chr1:147665926
|
T | A | 1 | a0001c0001t0008g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+3904A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665926 | ||||||
chr1:147666072
|
G | A | 1 | a0001c0002t0002g0038 | 2 | HG02027.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219+3758C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666072 | ||||||
chr1:147666206
|
C | T | 1 | a0001c0003t0018g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.219+3624G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666206 | ||||||
chr1:147666331
|
G | T | 1 | a0001c0003t0045g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+3499C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666331 | ||||||
chr1:147666481
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.219+3349C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666481 | ||||||
chr1:147666583
|
G | A | 1 | a0001c0003t0003g0130 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.219+3247C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666583 | ||||||
chr1:147666691
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(98): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.219+3139G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666691 | ||||||
chr1:147666696
|
CAATTA | C | 3 | a0001c0003t0003g0027a0001c0003t0003g0131a0001c0003t0057g0132 | 5 | NA18982.hp1 NA18986.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+3129_219+3133d others(7): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666696 | ||||||
chr1:147666712
|
C | T | 1 | a0001c0001t0034g0049 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219+3118G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666712 | ||||||
chr1:147666777
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(46): Show | 119 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.219+3053C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666777 | ||||||
chr1:147667102
|
GA | G | 3 | a0001c0001t0004g0035a0001c0001t0004g0069a0001c0001t0004g0070 | 4 | HG00639.hp1 HG00735.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+2727delT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667102 | ||||||
chr1:147667224
|
G | GT | 185 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(182): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.219+2605dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667224 | ||||||
chr1:147667377
|
C | T | 1 | a0001c0003t0003g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.219+2453G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667377 | ||||||
chr1:147667437
|
C | T | 1 | a0001c0003t0003g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.219+2393G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667437 | ||||||
chr1:147667786
|
T | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(98): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.219+2044A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667786 | ||||||
chr1:147667882
|
C | T | 1 | a0001c0002t0002g0034 | 2 | NA18953.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.219+1948G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667882 | ||||||
chr1:147667931
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(104): Show | 240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.219+1899C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667931 | ||||||
chr1:147667988
|
C | CA | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(178): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.219+1841dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667988 | ||||||
chr1:147668073
|
A | G | 1 | a0004c0006t0022g0033 | 2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.219+1757T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668073 | ||||||
chr1:147668334
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(53): Show | 127 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.219+1496C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668334 | ||||||
chr1:147668399
|
T | G | 9 | a0001c0001t0013g0024a0001c0001t0013g0106a0001c0002t0002g0019others(6): Show | 17 | HG00639.hp2 HG01109.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.219+1431A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668399 | ||||||
chr1:147668408
|
C | A | 2 | a0001c0003t0018g0046a0001c0003t0018g0182 | 3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219+1422G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668408 | ||||||
chr1:147668415
|
G | GAT | 29 | a0001c0001t0004g0067a0001c0001t0011g0018a0001c0001t0011g0056others(26): Show | 59 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+1413_219+1414d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668415 | ||||||
chr1:147668415
|
GAT | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(50): Show | 124 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.219+1413_219+1414d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668415 | ||||||
chr1:147668828
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.219+1002G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668828 | ||||||
chr1:147668829
|
G | A | 4 | a0001c0002t0033g0058a0001c0003t0006g0021a0001c0003t0006g0059others(1): Show | 6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+1001C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668829 | ||||||
chr1:147669040
|
C | T | 3 | a0001c0001t0049g0064a0001c0003t0045g0062a0001c0003t0047g0063 | 3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669040 | ||||||
chr1:147669073
|
A | T | 1 | a0001c0003t0003g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.219+757T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669073 | ||||||
chr1:147669081
|
G | T | 1 | a0001c0003t0019g0031 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.219+749C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669081 | ||||||
chr1:147669092
|
A | AT | 111 | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0016others(108): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.219+737dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669092 | ||||||
chr1:147669271
|
C | CA | 184 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(181): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.219+558dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669271 | ||||||
chr1:147669340
|
T | C | 1 | a0001c0001t0004g0016 | 5 | NA18973.hp1 NA18981.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+490A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669340 | ||||||
chr1:147669579
|
C | A | 1 | a0001c0003t0003g0183 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.219+251G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669579 | ||||||
chr1:147669688
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(99): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.219+142G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669688 | ||||||
chr1:147669798
|
C | T | 3 | a0001c0001t0049g0064a0001c0003t0045g0062a0001c0003t0047g0063 | 3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+32G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669798 |