geneid | 55156 |
---|---|
ensemblid | ENSG00000104442.10 |
hgncid | 17684 |
symbol | ARMC1 |
name | armadillo repeat containing 1 |
refseq_nuc | NM_018120.6 |
refseq_prot | NP_060590.1 |
ensembl_nuc | ENST00000276569.8 |
ensembl_prot | ENSP00000276569.3 |
mane_status | MANE Select |
chr | chr8 |
start | 65602458 |
end | 65634177 |
strand | - |
ver | v1.2 |
region | chr8:65602458-65634177 |
region5000 | chr8:65597458-65639177 |
regionname0 | ARMC1_chr8_65602458_65634177 |
regionname5000 | ARMC1_chr8_65597458_65639177 |
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 | 282 | 388 | 90 | 74 | 160 | 18 | 44 | 129 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0002 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0003 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 849 | 233 | 76 | 42 | 76 | 6 | 32 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
c0002 | 0/1 | 849 | 135 | 12 | 27 | 73 | 11 | 11 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
c0003 | 0/0 | 849 | 16 | 2 | 5 | 7 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
c0004 | 0/0 | 849 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
c0005 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
c0006 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
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 | 2152 | 100 | 9 | 10 | 59 | 0 | 22 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0002 | 0/1 | 2153 | 94 | 3 | 15 | 62 | 5 | 8 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0003 | 0/0 | 2152 | 93 | 52 | 28 | 0 | 6 | 7 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0004 | 0/0 | 2153 | 49 | 9 | 9 | 20 | 7 | 4 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0005 | 0/0 | 2153 | 19 | 5 | 2 | 12 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0006 | 0/0 | 2152 | 8 | 8 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0007 | 0/0 | 2154 | 6 | 0 | 6 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0008 | 0/0 | 2153 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0009 | 0/0 | 2154 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0010 | 0/0 | 2152 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0011 | 0/0 | 2152 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0012 | 0/0 | 2153 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0013 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0014 | 0/0 | 2152 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0015 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0016 | 1/0 | 2152 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0017 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0018 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0019 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0020 | 0/0 | 2152 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0021 | 0/0 | 2152 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0022 | 0/0 | 2152 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
t0023 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
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 | 17 | 2 | 2 | 13 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0002 | 0/0 | 9 | 1 | 1 | 5 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0003 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 849 | 233 | 76 | 42 | 76 | 6 | 32 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002 | 0/1 | 849 | 135 | 12 | 27 | 73 | 11 | 11 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0003 | 0/0 | 849 | 16 | 2 | 5 | 7 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0004 | 0/0 | 849 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0002c0006 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0003c0005 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3000 | 99 | 9 | 10 | 58 | 0 | 22 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0003 | 0/0 | 3000 | 92 | 51 | 28 | 0 | 6 | 7 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0005 | 0/0 | 3001 | 19 | 5 | 2 | 12 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0006 | 0/0 | 3000 | 8 | 8 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0008 | 0/0 | 3001 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0010 | 0/0 | 3000 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0011 | 0/0 | 3000 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0015 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0016 | 1/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0017 | 0/0 | 3002 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0018 | 0/0 | 3001 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0020 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0021 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0022 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0001t0023 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0002 | 0/1 | 3001 | 93 | 3 | 15 | 61 | 5 | 8 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0003 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0004 | 0/0 | 3001 | 29 | 7 | 4 | 9 | 6 | 3 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0007 | 0/0 | 3002 | 6 | 0 | 6 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0009 | 0/0 | 3002 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0012 | 0/0 | 3001 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0013 | 0/0 | 3001 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0014 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0002t0019 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0003t0004 | 0/0 | 3001 | 16 | 2 | 5 | 7 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0001c0004t0004 | 0/0 | 3001 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0002c0006t0001 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
a0003c0005t0002 | 0/0 | 3001 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | copy fasta | chr8 | 65597458 | 65639177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 5 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0003 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0010g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0011g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0016g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0017g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0018g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0020g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0021g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0022g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0001t0023g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0001 | 0/0 | 17 | 2 | 2 | 13 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0012g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0014g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0002t0019g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0004t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0001c0004t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0002c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
a0003c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0213 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0273 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00140 | hp1 | a0001 | c0002 | t0004 | g0318 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00140 | hp2 | a0001 | c0003 | t0004 | g0292 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00280 | hp1 | a0001 | c0002 | t0004 | g0279 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0107 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0274 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0287 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0272 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00733 | hp2 | a0001 | c0001 | t0010 | g0281 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00735 | hp1 | a0001 | c0002 | t0007 | g0269 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00741 | hp1 | a0001 | c0002 | t0014 | g0080 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG00741 | hp2 | a0001 | c0002 | t0007 | g0267 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0317 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01074 | hp2 | a0001 | c0001 | t0010 | g0283 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0277 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01168 | hp2 | a0001 | c0003 | t0004 | g0296 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01175 | hp1 | a0001 | c0002 | t0004 | g0280 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01192 | hp2 | a0001 | c0002 | t0007 | g0261 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01255 | hp2 | a0001 | c0002 | t0004 | g0275 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01346 | hp1 | a0001 | c0003 | t0004 | g0291 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01496 | hp2 | a0001 | c0003 | t0004 | g0011 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0014 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0103 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0235 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01516 | hp2 | a0001 | c0002 | t0004 | g0031 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0236 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0014 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01928 | hp2 | a0001 | c0002 | t0007 | g0252 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01943 | hp2 | a0001 | c0002 | t0007 | g0259 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0260 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02027 | hp1 | a0002 | c0006 | t0001 | g0176 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0254 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02155 | hp2 | a0001 | c0001 | t0011 | g0160 | EAS | CDX | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0276 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02293 | hp1 | a0001 | c0002 | t0012 | g0069 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02293 | hp2 | a0001 | c0003 | t0004 | g0290 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0207 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02602 | hp2 | a0001 | c0002 | t0004 | g0031 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0268 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02698 | hp1 | a0001 | c0002 | t0004 | g0030 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0074 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0304 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0271 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0265 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0321 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0285 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0309 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03704 | hp2 | a0001 | c0001 | t0022 | g0193 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03831 | hp2 | a0001 | c0001 | t0011 | g0171 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03834 | hp2 | a0001 | c0002 | t0004 | g0251 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04115 | hp2 | a0001 | c0003 | t0004 | g0293 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04204 | hp2 | a0001 | c0001 | t0020 | g0282 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0316 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18939 | hp2 | a0001 | c0003 | t0004 | g0298 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18942 | hp2 | a0001 | c0004 | t0004 | g0032 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18943 | hp1 | a0003 | c0005 | t0002 | g0047 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18946 | hp2 | a0001 | c0004 | t0004 | g0284 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18950 | hp2 | a0001 | c0001 | t0008 | g0144 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18951 | hp2 | a0001 | c0003 | t0004 | g0294 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18956 | hp1 | a0001 | c0002 | t0009 | g0077 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18960 | hp2 | a0001 | c0001 | t0021 | g0153 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18965 | hp2 | a0001 | c0003 | t0004 | g0289 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18967 | hp1 | a0001 | c0002 | t0009 | g0061 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18967 | hp2 | a0001 | c0004 | t0004 | g0286 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18972 | hp2 | a0001 | c0002 | t0013 | g0060 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18977 | hp2 | a0001 | c0004 | t0004 | g0032 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18989 | hp2 | a0001 | c0002 | t0004 | g0264 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18997 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18997 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19001 | hp2 | a0001 | c0003 | t0004 | g0288 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19043 | hp1 | a0001 | c0001 | t0015 | g0036 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19056 | hp1 | a0001 | c0003 | t0004 | g0295 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19067 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19074 | hp2 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19078 | hp1 | a0001 | c0001 | t0017 | g0299 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19079 | hp2 | a0001 | c0002 | t0004 | g0270 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19080 | hp2 | a0001 | c0002 | t0004 | g0256 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19081 | hp1 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19086 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19088 | hp2 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA19240 | hp2 | a0001 | c0002 | t0019 | g0250 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ASW | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ASW | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0278 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0297 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0076 | REF | REF | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0016 | g0086 | REF | REF | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:65604468
|
C | T | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.775G>A | p.Gly259Ser | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 990/3000 | 775/849 | 259/282 | chr8 | 65604468 | ||
chr8:65627376
|
A | G | 1 | a0003 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.23T>C | p.Met8Thr | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/7 | 238/3000 | 23/849 | 8/282 | chr8 | 65627376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:65604427
|
A | T | 1 | a0001c0004 | 4 | NA18942.hp2 NA18946.hp2 NA18967.hp2 others(1): Show |
synonymous_variant | LOW | c.816T>A | p.Ala272Ala | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1031/3000 | 816/849 | 272/282 | chr8 | 65604427 | ||
chr8:65605314
|
T | C | 2 | a0001c0003a0001c0004 | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
synonymous_variant | LOW | c.606A>G | p.Ser202Ser | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/7 | 821/3000 | 606/849 | 202/282 | chr8 | 65605314 | ||
chr8:65613313
|
T | C | 2 | a0001c0002a0003c0005 | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
synonymous_variant | LOW | c.396A>G | p.Gln132Gln | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/7 | 611/3000 | 396/849 | 132/282 | chr8 | 65613313 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:65602534
|
T | A | 1 | a0001c0002t0012 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1860 | chr8 | 65602534 | |||||
chr8:65602545
|
A | G | 3 | a0001c0001t0005a0001c0001t0017a0001c0001t0018 | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1849T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1849 | chr8 | 65602545 | |||||
chr8:65602553
|
T | C | 1 | a0001c0002t0013 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1841A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1841 | chr8 | 65602553 | |||||
chr8:65602619
|
C | T | 1 | a0001c0001t0018 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1775 | chr8 | 65602619 | |||||
chr8:65602719
|
T | C | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0017others(13): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1675A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1675 | chr8 | 65602719 | |||||
chr8:65602730
|
T | C | 14 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(11): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1664 | chr8 | 65602730 | |||||
chr8:65602779
|
T | C | 1 | a0001c0001t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1615A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1615 | chr8 | 65602779 | |||||
chr8:65602828
|
G | GT | 10 | a0001c0001t0005a0001c0001t0008a0001c0001t0018others(7): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1565dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1565 | chr8 | 65602828 | |||||
chr8:65602828
|
G | GTT | 3 | a0001c0001t0017a0001c0002t0007a0001c0002t0009 | 9 | HG00735.hp1 HG00741.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1564_*1565dupAA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1565 | chr8 | 65602828 | |||||
chr8:65602828
|
G | T | 2 | a0001c0001t0010a0001c0001t0020 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1566 | chr8 | 65602828 | |||||
chr8:65602851
|
G | A | 2 | a0001c0001t0010a0001c0001t0020 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1543C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1543 | chr8 | 65602851 | |||||
chr8:65603102
|
C | G | 1 | a0001c0001t0021 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1292 | chr8 | 65603102 | |||||
chr8:65603333
|
T | C | 1 | a0001c0001t0020 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1061 | chr8 | 65603333 | |||||
chr8:65603548
|
G | A | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0017others(13): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*846C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 846 | chr8 | 65603548 | |||||
chr8:65603630
|
A | G | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0017others(13): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*764T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 764 | chr8 | 65603630 | |||||
chr8:65603753
|
C | T | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0017others(13): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 641 | chr8 | 65603753 | |||||
chr8:65603831
|
T | G | 3 | a0001c0001t0005a0001c0001t0017a0001c0001t0018 | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*563A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 563 | chr8 | 65603831 | |||||
chr8:65603839
|
C | T | 1 | a0001c0001t0011 | 2 | HG02155.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*555G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 555 | chr8 | 65603839 | |||||
chr8:65603852
|
G | T | 3 | a0001c0001t0005a0001c0001t0017a0001c0001t0018 | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*542C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 542 | chr8 | 65603852 | |||||
chr8:65604255
|
C | T | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(19): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*139G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 139 | chr8 | 65604255 | |||||
chr8:65627405
|
T | C | 1 | a0001c0001t0022 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/7 | 7 | chr8 | 65627405 | |||||
chr8:65634122
|
G | A | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(16): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
5_prime_UTR_variant | MODIFIER | c.-160C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/7 | 6724 | chr8 | 65634122 | |||||
chr8:65634172
|
G | A | 1 | a0001c0001t0023 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/7 | 6774 | chr8 | 65634172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:65604854
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.658-269G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65604854 | ||||||
chr8:65605000
|
G | A | 1 | a0001c0002t0013g0060 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.657+263C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605000 | ||||||
chr8:65605219
|
T | C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.657+44A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605219 | ||||||
chr8:65605251
|
C | T | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.657+12G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605251 | ||||||
chr8:65605619
|
G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466-81C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605619 | ||||||
chr8:65605778
|
A | AT | 7 | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0003g0199others(4): Show | 7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-241dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605778 | ||||||
chr8:65605848
|
A | G | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.466-310T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605848 | ||||||
chr8:65606227
|
G | A | 142 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(139): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.466-689C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606227 | ||||||
chr8:65606241
|
G | A | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-703C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606241 | ||||||
chr8:65606242
|
T | G | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-704A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606242 | ||||||
chr8:65606243
|
C | T | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-705G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606243 | ||||||
chr8:65606360
|
C | CA | 154 | a0001c0001t0001g0154a0001c0001t0003g0009a0001c0001t0003g0023others(151): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.466-823dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606360 | ||||||
chr8:65606371
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.466-833T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606371 | ||||||
chr8:65606387
|
A | G | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-849T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606387 | ||||||
chr8:65606392
|
T | G | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.466-854A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606392 | ||||||
chr8:65606603
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.466-1065A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606603 | ||||||
chr8:65606651
|
G | A | 10 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0237others(7): Show | 12 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-1113C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606651 | ||||||
chr8:65606766
|
A | G | 146 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(143): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.466-1228T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606766 | ||||||
chr8:65606807
|
C | T | 22 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0044others(19): Show | 26 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.466-1269G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606807 | ||||||
chr8:65606812
|
T | C | 1 | a0001c0002t0002g0096 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.466-1274A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606812 | ||||||
chr8:65607024
|
C | T | 146 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(143): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.466-1486G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607024 | ||||||
chr8:65607157
|
C | T | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.466-1619G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607157 | ||||||
chr8:65607322
|
T | G | 2 | a0001c0001t0006g0040a0001c0001t0006g0041 | 2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.466-1784A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607322 | ||||||
chr8:65607454
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.466-1916G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607454 | ||||||
chr8:65607636
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-2098G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607636 | ||||||
chr8:65607804
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2266A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607804 | ||||||
chr8:65608017
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2479A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608017 | ||||||
chr8:65608040
|
G | A | 2 | a0001c0001t0006g0037a0001c0001t0015g0036 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.466-2502C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608040 | ||||||
chr8:65608239
|
A | T | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.466-2701T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608239 | ||||||
chr8:65608389
|
C | T | 2 | a0001c0001t0003g0190a0001c0001t0003g0205 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.466-2851G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608389 | ||||||
chr8:65608455
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2917C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608455 | ||||||
chr8:65608486
|
G | A | 1 | a0001c0001t0010g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.466-2948C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608486 | ||||||
chr8:65608521
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466-2983A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608521 | ||||||
chr8:65608626
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3088A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608626 | ||||||
chr8:65608666
|
G | C | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-3128C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608666 | ||||||
chr8:65608698
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0137a0001c0001t0001g0161others(1): Show | 5 | HG03017.hp1 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-3160T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608698 | ||||||
chr8:65608715
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0167others(1): Show | 4 | NA18957.hp2 NA18961.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-3177G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608715 | ||||||
chr8:65608767
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3229C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608767 | ||||||
chr8:65608787
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3249A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608787 | ||||||
chr8:65608814
|
CAGG | C | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.466-3279_466-3277d others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608814 | ||||||
chr8:65609037
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.466-3499G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609037 | ||||||
chr8:65609074
|
C | CT | 146 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(143): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.466-3537dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609074 | ||||||
chr8:65609104
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3566G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609104 | ||||||
chr8:65609106
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3568A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609106 | ||||||
chr8:65609133
|
CT | C | 171 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0152others(168): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.466-3596delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609133 | ||||||
chr8:65609157
|
G | A | 1 | a0001c0002t0004g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.466-3619C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609157 | ||||||
chr8:65609176
|
T | G | 146 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(143): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.466-3638A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609176 | ||||||
chr8:65609204
|
G | A | 6 | a0001c0001t0003g0010a0001c0001t0003g0232a0001c0001t0003g0233others(3): Show | 8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-3666C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609204 | ||||||
chr8:65609225
|
C | A | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-3687G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609225 | ||||||
chr8:65609236
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.466-3698C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609236 | ||||||
chr8:65609237
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.466-3699T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609237 | ||||||
chr8:65609261
|
C | A | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.466-3723G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609261 | ||||||
chr8:65609297
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.466-3759C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609297 | ||||||
chr8:65609397
|
A | G | 1 | a0001c0002t0002g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.465+3847T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609397 | ||||||
chr8:65609409
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.465+3835T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609409 | ||||||
chr8:65609534
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3710A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609534 | ||||||
chr8:65609625
|
C | A | 1 | a0001c0001t0003g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.465+3619G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609625 | ||||||
chr8:65609631
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.465+3613C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609631 | ||||||
chr8:65609655
|
C | T | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+3589G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609655 | ||||||
chr8:65609686
|
C | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0130others(8): Show | 11 | HG02080.hp2 HG02135.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.465+3558G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609686 | ||||||
chr8:65609716
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3528C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609716 | ||||||
chr8:65609872
|
A | AAAAG | 76 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(73): Show | 91 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | ||||||
chr8:65609872
|
A | AAAG | 8 | a0001c0001t0003g0235a0001c0001t0010g0281a0001c0001t0010g0283others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | ||||||
chr8:65609872
|
A | AAG | 124 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0037others(121): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | ||||||
chr8:65609872
|
A | AG | 23 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(20): Show | 24 | HG01069.hp1 HG01167.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | ||||||
chr8:65609872
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.465+3372T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | ||||||
chr8:65609877
|
G | A | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.465+3367C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609877 | ||||||
chr8:65609879
|
A | AAAAG | 231 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(228): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.465+3364_465+3365i others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609879 | ||||||
chr8:65609879
|
A | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.465+3365T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609879 | ||||||
chr8:65609882
|
G | A | 232 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(229): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.465+3362C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609882 | ||||||
chr8:65609882
|
G | GAAAAAGA others(2): Show |
5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0229others(2): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+3353_465+3361d others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609882 | ||||||
chr8:65609888
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3356C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609888 | ||||||
chr8:65609889
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3355T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609889 | ||||||
chr8:65610009
|
T | C | 5 | a0001c0001t0006g0034a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG02965.hp1 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+3235A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610009 | ||||||
chr8:65610010
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465+3234A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610010 | ||||||
chr8:65610090
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3154C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610090 | ||||||
chr8:65610102
|
A | AT | 151 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(148): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.465+3141dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610102 | ||||||
chr8:65610108
|
T | TG | 3 | a0001c0004t0004g0032a0001c0004t0004g0284a0001c0004t0004g0286 | 4 | NA18942.hp2 NA18946.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+3135_465+3136i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610108 | ||||||
chr8:65610120
|
C | T | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.465+3124G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610120 | ||||||
chr8:65610159
|
G | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3085C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610159 | ||||||
chr8:65610172
|
A | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3072T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610172 | ||||||
chr8:65610183
|
C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3061G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610183 | ||||||
chr8:65610191
|
A | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3053T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610191 | ||||||
chr8:65610200
|
C | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3044G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610200 | ||||||
chr8:65610201
|
G | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3043C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610201 | ||||||
chr8:65610202
|
A | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3042T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610202 | ||||||
chr8:65610204
|
T | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3040A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610204 | ||||||
chr8:65610211
|
A | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3033T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610211 | ||||||
chr8:65610222
|
T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3022A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610222 | ||||||
chr8:65610235
|
T | C | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.465+3009A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610235 | ||||||
chr8:65610242
|
C | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3002G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610242 | ||||||
chr8:65610243
|
G | A | 2 | a0001c0002t0004g0275a0001c0002t0004g0279 | 2 | HG00280.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.465+3001C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610243 | ||||||
chr8:65610243
|
G | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3001C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610243 | ||||||
chr8:65610244
|
T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3000A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610244 | ||||||
chr8:65610247
|
A | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2997T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610247 | ||||||
chr8:65610259
|
T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2985A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610259 | ||||||
chr8:65610263
|
T | A | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+2981A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610263 | ||||||
chr8:65610296
|
A | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2948T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610296 | ||||||
chr8:65610302
|
T | A | 3 | a0001c0001t0003g0242a0001c0001t0003g0243a0001c0001t0003g0244 | 3 | HG02145.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.465+2942A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610302 | ||||||
chr8:65610309
|
G | A | 320 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.465+2935C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610309 | ||||||
chr8:65610337
|
T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2907A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610337 | ||||||
chr8:65610338
|
C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2906G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610338 | ||||||
chr8:65610348
|
C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2896G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610348 | ||||||
chr8:65610351
|
C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2893G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610351 | ||||||
chr8:65610427
|
G | A | 132 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0037others(129): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.465+2817C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610427 | ||||||
chr8:65610453
|
T | TG | 320 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.465+2790dupC | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610453 | ||||||
chr8:65610567
|
C | T | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+2677G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610567 | ||||||
chr8:65610606
|
A | G | 16 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(13): Show | 17 | HG02027.hp2 HG02055.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+2638T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610606 | ||||||
chr8:65610627
|
G | A | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+2617C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610627 | ||||||
chr8:65610657
|
C | T | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.465+2587G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610657 | ||||||
chr8:65610674
|
A | C | 1 | a0001c0002t0002g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.465+2570T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610674 | ||||||
chr8:65610744
|
G | A | 7 | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0003g0199others(4): Show | 7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+2500C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610744 | ||||||
chr8:65611036
|
C | T | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+2208G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611036 | ||||||
chr8:65611210
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+2034G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611210 | ||||||
chr8:65611230
|
G | A | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.465+2014C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611230 | ||||||
chr8:65611326
|
A | C | 1 | a0001c0001t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.465+1918T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611326 | ||||||
chr8:65611444
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.465+1800G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611444 | ||||||
chr8:65611482
|
CT | C | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+1761delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611482 | ||||||
chr8:65611517
|
C | G | 232 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(229): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.465+1727G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611517 | ||||||
chr8:65611564
|
C | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.465+1680G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611564 | ||||||
chr8:65611649
|
T | C | 31 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0026others(28): Show | 39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.465+1595A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611649 | ||||||
chr8:65611735
|
A | G | 1 | a0001c0002t0007g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.465+1509T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611735 | ||||||
chr8:65611810
|
G | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.465+1434C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611810 | ||||||
chr8:65611843
|
A | G | 155 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(152): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.465+1401T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611843 | ||||||
chr8:65611889
|
T | G | 1 | a0001c0002t0002g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.465+1355A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611889 | ||||||
chr8:65612028
|
C | T | 72 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0005others(69): Show | 99 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.465+1216G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612028 | ||||||
chr8:65612211
|
G | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465+1033C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612211 | ||||||
chr8:65612554
|
A | T | 1 | a0001c0002t0002g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.465+690T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612554 | ||||||
chr8:65612669
|
C | G | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+575G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612669 | ||||||
chr8:65612948
|
T | G | 1 | a0001c0001t0018g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.465+296A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612948 | ||||||
chr8:65612960
|
T | C | 6 | a0001c0002t0004g0254a0001c0002t0004g0257a0001c0002t0004g0263others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+284A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612960 | ||||||
chr8:65612967
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.465+277A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612967 | ||||||
chr8:65613630
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-197G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613630 | ||||||
chr8:65613712
|
A | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.276-279T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613712 | ||||||
chr8:65613889
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.276-456C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613889 | ||||||
chr8:65613921
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.276-488G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613921 | ||||||
chr8:65613959
|
C | CA | 170 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 206 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.276-527dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613959 | ||||||
chr8:65613959
|
CA | C | 71 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(68): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.276-527delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613959 | ||||||
chr8:65613974
|
C | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-541G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613974 | ||||||
chr8:65614243
|
A | G | 1 | a0001c0002t0009g0077 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.276-810T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614243 | ||||||
chr8:65614418
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.276-985T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614418 | ||||||
chr8:65614425
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.276-992T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614425 | ||||||
chr8:65614623
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.276-1190A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614623 | ||||||
chr8:65614647
|
T | G | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.276-1214A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614647 | ||||||
chr8:65614849
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.276-1416C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614849 | ||||||
chr8:65615040
|
TA | T | 15 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(12): Show | 17 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.276-1608delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615040 | ||||||
chr8:65615105
|
C | G | 2 | a0001c0002t0004g0256a0001c0002t0004g0258 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.276-1672G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615105 | ||||||
chr8:65615119
|
G | T | 1 | a0001c0001t0010g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.276-1686C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615119 | ||||||
chr8:65615193
|
A | C | 1 | a0001c0001t0006g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.276-1760T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615193 | ||||||
chr8:65615219
|
G | A | 2 | a0001c0003t0004g0288a0001c0003t0004g0298 | 2 | NA18939.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.276-1786C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615219 | ||||||
chr8:65615399
|
T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1966A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615399 | ||||||
chr8:65615400
|
TA | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 110 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.276-1968delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615400 | ||||||
chr8:65615400
|
TAA | T | 154 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(151): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.276-1969_276-1968d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615400 | ||||||
chr8:65615401
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1968T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615401 | ||||||
chr8:65615413
|
A | C | 1 | a0001c0002t0002g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.276-1980T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615413 | ||||||
chr8:65615413
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1980T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615413 | ||||||
chr8:65615416
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1983T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615416 | ||||||
chr8:65615419
|
A | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1986T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615419 | ||||||
chr8:65615420
|
C | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1987G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615420 | ||||||
chr8:65615421
|
A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1988T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615421 | ||||||
chr8:65615427
|
G | A | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276-1994C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615427 | ||||||
chr8:65615474
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.276-2041C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615474 | ||||||
chr8:65615479
|
T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2046A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615479 | ||||||
chr8:65615480
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2047C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615480 | ||||||
chr8:65615485
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2052T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615485 | ||||||
chr8:65615525
|
C | T | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.276-2092G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615525 | ||||||
chr8:65615646
|
G | T | 1 | a0001c0001t0003g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.276-2213C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615646 | ||||||
chr8:65615666
|
G | A | 1 | a0001c0002t0002g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-2233C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615666 | ||||||
chr8:65615826
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-2393G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615826 | ||||||
chr8:65615834
|
G | A | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.276-2401C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615834 | ||||||
chr8:65615891
|
G | A | 1 | a0001c0001t0020g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.276-2458C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615891 | ||||||
chr8:65615905
|
A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2472T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615905 | ||||||
chr8:65615906
|
G | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2473C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615906 | ||||||
chr8:65615908
|
A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2475T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615908 | ||||||
chr8:65616021
|
A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2588T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616021 | ||||||
chr8:65616031
|
T | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2598A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616031 | ||||||
chr8:65616093
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2660T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616093 | ||||||
chr8:65616119
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2686T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616119 | ||||||
chr8:65616128
|
G | GT | 7 | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0003g0199others(4): Show | 7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.276-2696dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616128 | ||||||
chr8:65616129
|
T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2696A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616129 | ||||||
chr8:65616164
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.276-2731C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616164 | ||||||
chr8:65616268
|
G | A | 2 | a0001c0002t0004g0276a0001c0002t0004g0278 | 2 | HG02280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.276-2835C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616268 | ||||||
chr8:65616279
|
C | T | 31 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0026others(28): Show | 39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.276-2846G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616279 | ||||||
chr8:65616299
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2866C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616299 | ||||||
chr8:65616322
|
A | G | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.276-2889T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616322 | ||||||
chr8:65616323
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-2890C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616323 | ||||||
chr8:65616369
|
G | A | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.276-2936C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616369 | ||||||
chr8:65616395
|
G | C | 1 | a0001c0001t0003g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.276-2962C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616395 | ||||||
chr8:65616403
|
G | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.276-2970C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616403 | ||||||
chr8:65616422
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-2989C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616422 | ||||||
chr8:65616442
|
G | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3009C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616442 | ||||||
chr8:65616456
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.276-3023C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616456 | ||||||
chr8:65616465
|
C | T | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.276-3032G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616465 | ||||||
chr8:65616492
|
C | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3059G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616492 | ||||||
chr8:65616553
|
A | AC | 11 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0005g0308others(8): Show | 11 | HG00544.hp1 HG02135.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.276-3121dupG | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616553 | ||||||
chr8:65616575
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.276-3142G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616575 | ||||||
chr8:65616576
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.276-3143C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616576 | ||||||
chr8:65616618
|
T | C | 1 | a0001c0001t0003g0028 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.276-3185A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616618 | ||||||
chr8:65616683
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3250C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616683 | ||||||
chr8:65616692
|
G | A | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3259C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616692 | ||||||
chr8:65616701
|
C | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3268G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616701 | ||||||
chr8:65616702
|
G | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3269C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616702 | ||||||
chr8:65616710
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3277T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616710 | ||||||
chr8:65616711
|
T | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3278A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616711 | ||||||
chr8:65616712
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3279T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616712 | ||||||
chr8:65616712
|
A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3279T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616712 | ||||||
chr8:65616734
|
T | C | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3301A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616734 | ||||||
chr8:65616742
|
G | A | 3 | a0001c0003t0004g0290a0001c0003t0004g0291a0001c0003t0004g0296 | 3 | HG01168.hp2 HG01346.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.276-3309C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616742 | ||||||
chr8:65616821
|
C | T | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-3388G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616821 | ||||||
chr8:65616854
|
C | T | 18 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0182others(15): Show | 21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3421G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616854 | ||||||
chr8:65616855
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.276-3422C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616855 | ||||||
chr8:65616866
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3433A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616866 | ||||||
chr8:65616902
|
G | A | 3 | a0001c0002t0002g0082a0001c0002t0002g0090a0001c0002t0002g0101 | 3 | NA18961.hp2 NA19011.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.276-3469C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616902 | ||||||
chr8:65616941
|
T | C | 2 | a0001c0002t0002g0079a0001c0002t0002g0083 | 2 | NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.276-3508A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616941 | ||||||
chr8:65616966
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-3533A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616966 | ||||||
chr8:65616970
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.276-3537G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616970 | ||||||
chr8:65616981
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0174 | 3 | HG02257.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.276-3548G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616981 | ||||||
chr8:65617016
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-3583C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617016 | ||||||
chr8:65617020
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.276-3587C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617020 | ||||||
chr8:65617032
|
C | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3599G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617032 | ||||||
chr8:65617143
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.276-3710G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617143 | ||||||
chr8:65617157
|
G | A | 1 | a0001c0002t0002g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-3724C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617157 | ||||||
chr8:65617172
|
G | A | 1 | a0001c0002t0002g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.276-3739C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617172 | ||||||
chr8:65617172
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3739C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617172 | ||||||
chr8:65617226
|
T | G | 1 | a0001c0001t0003g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.276-3793A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617226 | ||||||
chr8:65617402
|
A | G | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.276-3969T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617402 | ||||||
chr8:65617408
|
A | C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-3975T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617408 | ||||||
chr8:65617467
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.276-4034A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617467 | ||||||
chr8:65617482
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.276-4049G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617482 | ||||||
chr8:65617568
|
C | G | 54 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(51): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.276-4135G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617568 | ||||||
chr8:65617593
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-4160C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617593 | ||||||
chr8:65617617
|
TA | T | 17 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(14): Show | 19 | HG01109.hp1 HG01169.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.276-4185delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617617 | ||||||
chr8:65617677
|
C | T | 1 | a0001c0001t0003g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.276-4244G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617677 | ||||||
chr8:65617730
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-4297C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617730 | ||||||
chr8:65617763
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-4330G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617763 | ||||||
chr8:65617834
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-4401A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617834 | ||||||
chr8:65617850
|
GA | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 218 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.275+4412delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617850 | ||||||
chr8:65617857
|
A | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.275+4406T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617857 | ||||||
chr8:65617922
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.275+4341C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | ||||||
chr8:65617922
|
G | GT | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4340_275+4341i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | ||||||
chr8:65617922
|
G | T | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.275+4341C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | ||||||
chr8:65617923
|
G | C | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.275+4340C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617923 | ||||||
chr8:65618009
|
G | A | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.275+4254C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618009 | ||||||
chr8:65618063
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4200C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618063 | ||||||
chr8:65618088
|
A | T | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.275+4175T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618088 | ||||||
chr8:65618104
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4159A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618104 | ||||||
chr8:65618147
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4116G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618147 | ||||||
chr8:65618150
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4113C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618150 | ||||||
chr8:65618157
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4106T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618157 | ||||||
chr8:65618248
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0117 | 2 | NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.275+4015G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618248 | ||||||
chr8:65618325
|
A | G | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.275+3938T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618325 | ||||||
chr8:65618345
|
A | G | 2 | a0001c0002t0002g0016a0001c0002t0002g0045 | 3 | HG00738.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.275+3918T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618345 | ||||||
chr8:65618386
|
G | A | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.275+3877C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618386 | ||||||
chr8:65618423
|
G | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+3840C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618423 | ||||||
chr8:65618447
|
G | A | 18 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0182others(15): Show | 21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+3816C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618447 | ||||||
chr8:65618521
|
C | CA | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 140 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.275+3741dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | ||||||
chr8:65618521
|
C | CAA | 54 | a0001c0001t0001g0108a0001c0001t0001g0143a0001c0001t0003g0003others(51): Show | 64 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.275+3740_275+3741d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | ||||||
chr8:65618521
|
CA | C | 8 | a0001c0001t0005g0308a0001c0001t0006g0034a0001c0002t0002g0071others(5): Show | 8 | HG00099.hp2 HG02965.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+3741delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | ||||||
chr8:65618548
|
T | C | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.275+3715A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618548 | ||||||
chr8:65618573
|
C | T | 1 | a0001c0002t0014g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.275+3690G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618573 | ||||||
chr8:65618576
|
G | C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.275+3687C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618576 | ||||||
chr8:65618595
|
A | AATTTCAG others(15): Show |
6 | a0001c0002t0002g0004a0001c0002t0002g0053a0001c0002t0002g0068others(3): Show | 9 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+3646_275+3667d others(24): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618595 | ||||||
chr8:65618674
|
G | C | 48 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0024others(45): Show | 58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.275+3589C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618674 | ||||||
chr8:65618710
|
T | C | 6 | a0001c0001t0003g0010a0001c0001t0003g0232a0001c0001t0003g0233others(3): Show | 8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+3553A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618710 | ||||||
chr8:65618772
|
G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+3491C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618772 | ||||||
chr8:65618857
|
T | G | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0184others(4): Show | 9 | HG01109.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.275+3406A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618857 | ||||||
chr8:65618903
|
C | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+3360G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618903 | ||||||
chr8:65618991
|
C | T | 1 | a0001c0001t0006g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.275+3272G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618991 | ||||||
chr8:65618997
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+3266G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618997 | ||||||
chr8:65619026
|
G | C | 1 | a0001c0001t0003g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.275+3237C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619026 | ||||||
chr8:65619394
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2869A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619394 | ||||||
chr8:65619413
|
A | G | 2 | a0001c0001t0003g0197a0001c0001t0003g0199 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.275+2850T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619413 | ||||||
chr8:65619542
|
G | GA | 18 | a0001c0002t0009g0077a0001c0003t0004g0011a0001c0003t0004g0285others(15): Show | 21 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+2720dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619542 | ||||||
chr8:65619561
|
G | A | 5 | a0001c0001t0006g0034a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG02965.hp1 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+2702C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619561 | ||||||
chr8:65619626
|
C | A | 1 | a0001c0003t0004g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.275+2637G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619626 | ||||||
chr8:65619626
|
C | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2637G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619626 | ||||||
chr8:65619644
|
C | T | 1 | a0003c0005t0002g0047 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.275+2619G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619644 | ||||||
chr8:65619668
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2595T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619668 | ||||||
chr8:65619801
|
T | C | 1 | a0001c0003t0004g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.275+2462A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619801 | ||||||
chr8:65619977
|
C | CA | 16 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0173others(13): Show | 16 | HG00673.hp2 HG01192.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.275+2285dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619977 | ||||||
chr8:65619977
|
CA | C | 7 | a0001c0001t0001g0152a0001c0001t0003g0200a0001c0001t0010g0281others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+2285delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619977 | ||||||
chr8:65620294
|
C | CT | 19 | a0001c0001t0005g0306a0001c0001t0017g0299a0001c0002t0002g0044others(16): Show | 19 | HG00408.hp1 HG02135.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.275+1968dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | ||||||
chr8:65620294
|
CT | C | 13 | a0001c0001t0005g0305a0001c0001t0006g0034a0001c0001t0006g0035others(10): Show | 13 | HG02486.hp1 HG02965.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.275+1968delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | ||||||
chr8:65620294
|
CTTTTT | C | 21 | a0001c0001t0001g0131a0001c0001t0001g0166a0001c0001t0003g0009others(18): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.275+1964_275+1968d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | ||||||
chr8:65620294
|
CTTTTTT | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 161 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.275+1963_275+1968d others(8): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | ||||||
chr8:65620294
|
CTTTTTTT | C | 14 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0028others(11): Show | 16 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.275+1962_275+1968d others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | ||||||
chr8:65620364
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.275+1899G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620364 | ||||||
chr8:65620388
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1875C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620388 | ||||||
chr8:65620455
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.275+1808G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620455 | ||||||
chr8:65620503
|
T | C | 9 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0037others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+1760A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620503 | ||||||
chr8:65620530
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1733A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620530 | ||||||
chr8:65620542
|
T | TC | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1720dupG | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620542 | ||||||
chr8:65620759
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275+1504G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620759 | ||||||
chr8:65620798
|
T | TAAAAAAA others(6): Show |
3 | a0001c0001t0003g0027a0001c0001t0003g0186a0001c0001t0003g0208 | 4 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1464_275+1465i others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620798 | ||||||
chr8:65620799
|
T | A | 3 | a0001c0001t0003g0027a0001c0001t0003g0186a0001c0001t0003g0208 | 4 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1464A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0150others(1): Show | 4 | HG01975.hp1 HG04115.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(4): Show |
73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(5): Show |
10 | a0001c0001t0001g0108a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 10 | HG01516.hp1 HG01517.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(14): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(6): Show |
32 | a0001c0001t0001g0121a0001c0001t0003g0003a0001c0001t0003g0010others(29): Show | 39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(7): Show |
38 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0024others(35): Show | 45 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620799
|
T | TAAAAAAA others(8): Show |
5 | a0001c0001t0003g0184a0001c0001t0003g0197a0001c0001t0003g0199others(2): Show | 5 | HG01255.hp1 HG01433.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(17): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | ||||||
chr8:65620949
|
T | G | 2 | a0001c0002t0002g0074a0001c0002t0002g0106 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.275+1314A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620949 | ||||||
chr8:65621071
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1192G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621071 | ||||||
chr8:65621084
|
C | T | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.275+1179G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621084 | ||||||
chr8:65621391
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.275+872T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621391 | ||||||
chr8:65621425
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.275+838G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621425 | ||||||
chr8:65621561
|
T | G | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+702A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621561 | ||||||
chr8:65621562
|
G | A | 48 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0024others(45): Show | 58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.275+701C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621562 | ||||||
chr8:65621670
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275+593C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621670 | ||||||
chr8:65621680
|
T | C | 29 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(26): Show | 30 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.275+583A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621680 | ||||||
chr8:65621683
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+580T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621683 | ||||||
chr8:65621711
|
G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+552C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621711 | ||||||
chr8:65621719
|
C | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+544G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621719 | ||||||
chr8:65621820
|
T | C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.275+443A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621820 | ||||||
chr8:65621977
|
G | A | 2 | a0001c0001t0001g0022a0001c0002t0002g0043 | 3 | HG00673.hp2 HG02257.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.275+286C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621977 | ||||||
chr8:65622006
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.275+257G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65622006 | ||||||
chr8:65622407
|
G | T | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.184-53C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622407 | ||||||
chr8:65622454
|
G | A | 2 | a0001c0001t0006g0037a0001c0001t0015g0036 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-100C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622454 | ||||||
chr8:65622552
|
C | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0137 | 3 | HG03491.hp1 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.184-198G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622552 | ||||||
chr8:65622566
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.184-212G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622566 | ||||||
chr8:65622712
|
A | G | 1 | a0001c0001t0020g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184-358T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622712 | ||||||
chr8:65622715
|
G | GAA | 164 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 200 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.184-363_184-362dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622715 | ||||||
chr8:65622725
|
A | C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-371T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622725 | ||||||
chr8:65622740
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-386G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622740 | ||||||
chr8:65622787
|
G | A | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-433C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622787 | ||||||
chr8:65622841
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.184-487T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622841 | ||||||
chr8:65622897
|
T | C | 1 | a0001c0001t0003g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.184-543A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622897 | ||||||
chr8:65623012
|
T | TA | 6 | a0001c0001t0001g0127a0001c0001t0001g0177a0001c0001t0005g0300others(3): Show | 6 | HG02055.hp2 HG02523.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-659dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623012 | ||||||
chr8:65623081
|
G | A | 48 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0024others(45): Show | 58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.184-727C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623081 | ||||||
chr8:65623165
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-811C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623165 | ||||||
chr8:65623231
|
C | T | 3 | a0001c0001t0006g0035a0001c0001t0006g0037a0001c0001t0015g0036 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-877G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623231 | ||||||
chr8:65623271
|
G | A | 1 | a0001c0002t0004g0270 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.184-917C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623271 | ||||||
chr8:65623307
|
C | CA | 11 | a0001c0002t0002g0053a0001c0002t0002g0054a0001c0002t0002g0074others(8): Show | 11 | HG01928.hp1 HG02602.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-954dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(2): Show |
91 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0018others(88): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.184-962_184-954dup others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(3): Show |
68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0017others(65): Show | 77 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.184-963_184-954dup others(10): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0148others(1): Show | 4 | HG02074.hp2 HG04204.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-964_184-954dup others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0159a0001c0001t0006g0034a0001c0001t0006g0039others(2): Show | 5 | HG02965.hp1 HG03540.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-965_184-954dup others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0006g0035a0001c0001t0006g0037a0001c0001t0006g0038others(4): Show | 7 | HG02486.hp1 HG02647.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-966_184-954dup others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(7): Show |
23 | a0001c0001t0005g0033a0001c0001t0005g0301a0001c0001t0005g0304others(20): Show | 25 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.184-967_184-954dup others(14): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(8): Show |
24 | a0001c0001t0005g0300a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 25 | HG00323.hp2 HG00735.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.184-968_184-954dup others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623307
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0005g0307a0001c0001t0005g0308a0001c0001t0018g0316others(2): Show | 5 | HG03834.hp2 NA18522.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-969_184-954dup others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | ||||||
chr8:65623324
|
A | AAAAAAAA others(6): Show |
7 | a0001c0003t0004g0287a0001c0003t0004g0288a0001c0003t0004g0289others(4): Show | 7 | HG00140.hp2 HG00642.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-971_184-970ins others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623324 | ||||||
chr8:65623324
|
A | AAAAAAAA others(5): Show |
10 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0290others(7): Show | 13 | HG01168.hp2 HG01346.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.184-971_184-970ins others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623324 | ||||||
chr8:65623499
|
C | T | 3 | a0001c0001t0005g0302a0001c0001t0005g0304a0001c0001t0005g0312 | 3 | HG02486.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.184-1145G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623499 | ||||||
chr8:65623504
|
G | A | 3 | a0001c0001t0003g0242a0001c0001t0003g0243a0001c0001t0003g0244 | 3 | HG02145.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.184-1150C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623504 | ||||||
chr8:65623721
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.184-1367T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623721 | ||||||
chr8:65623732
|
T | TA | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1379dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623732 | ||||||
chr8:65623755
|
C | T | 18 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0182others(15): Show | 21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-1401G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623755 | ||||||
chr8:65623786
|
C | CT | 72 | a0001c0001t0005g0033a0001c0001t0005g0304a0001c0001t0005g0306others(69): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-1433dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTT | 24 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0302others(21): Show | 24 | HG01175.hp1 HG01192.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.184-1434_184-1433d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTTTT | 34 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0025others(31): Show | 44 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.184-1436_184-1433d others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTTTTT | 40 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(37): Show | 45 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.184-1437_184-1433d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTTTTTT | 56 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.184-1438_184-1433d others(8): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTTTTTTT | 28 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(25): Show | 34 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.184-1439_184-1433d others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0163others(3): Show | 6 | HG00621.hp2 HG02027.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1440_184-1433d others(10): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623786
|
CTTTTTTT others(10): Show |
C | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-1449_184-1433d others(19): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | ||||||
chr8:65623892
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1538T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623892 | ||||||
chr8:65623900
|
C | T | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.184-1546G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623900 | ||||||
chr8:65623938
|
T | C | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.184-1584A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623938 | ||||||
chr8:65623956
|
C | T | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.184-1602G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623956 | ||||||
chr8:65624049
|
C | T | 9 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0037others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-1695G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624049 | ||||||
chr8:65624090
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.184-1736C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624090 | ||||||
chr8:65624175
|
C | A | 1 | a0001c0002t0002g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.184-1821G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624175 | ||||||
chr8:65624327
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1973A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624327 | ||||||
chr8:65624423
|
C | T | 1 | a0001c0002t0004g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.184-2069G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624423 | ||||||
chr8:65624434
|
G | C | 1 | a0001c0002t0004g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184-2080C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624434 | ||||||
chr8:65624456
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0137a0001c0001t0001g0161others(1): Show | 5 | HG03017.hp1 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2102C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624456 | ||||||
chr8:65624466
|
T | G | 3 | a0001c0003t0004g0289a0001c0003t0004g0294a0001c0003t0004g0295 | 3 | NA18951.hp2 NA18965.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.184-2112A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624466 | ||||||
chr8:65624498
|
C | CA | 28 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(25): Show | 31 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2145dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624498
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0228 | 3 | HG01070.hp2 HG02818.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.184-2157_184-2145d others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624498
|
C | CAAAAAAA others(7): Show |
23 | a0001c0001t0001g0119a0001c0001t0001g0140a0001c0001t0001g0177others(20): Show | 31 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624498
|
C | CAAAAAAA others(8): Show |
91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 112 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(17): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624498
|
C | CAAAAAAA others(9): Show |
27 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0124others(24): Show | 32 | HG00597.hp1 HG01106.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(18): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624498
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0003g0241a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(19): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | ||||||
chr8:65624757
|
ATAAAT | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.184-2408_184-2404d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624757 | ||||||
chr8:65624780
|
TG | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-2427delC | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624780 | ||||||
chr8:65624783
|
A | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-2429T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624783 | ||||||
chr8:65624848
|
T | A | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+2368A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624848 | ||||||
chr8:65624885
|
C | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+2331G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624885 | ||||||
chr8:65625027
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.183+2189T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625027 | ||||||
chr8:65625291
|
C | T | 1 | a0001c0001t0003g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.183+1925G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625291 | ||||||
chr8:65625298
|
T | C | 1 | a0001c0002t0002g0072 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.183+1918A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625298 | ||||||
chr8:65625321
|
G | T | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1895C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625321 | ||||||
chr8:65625358
|
G | T | 17 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(14): Show | 20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.183+1858C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625358 | ||||||
chr8:65625385
|
G | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.183+1831C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625385 | ||||||
chr8:65625440
|
C | T | 18 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0182others(15): Show | 21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.183+1776G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625440 | ||||||
chr8:65625606
|
C | T | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.183+1610G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625606 | ||||||
chr8:65625664
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+1552T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625664 | ||||||
chr8:65625739
|
T | C | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183+1477A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625739 | ||||||
chr8:65625798
|
T | C | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(13): Show | 18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+1418A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625798 | ||||||
chr8:65625826
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.183+1390A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625826 | ||||||
chr8:65625829
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183+1387G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625829 | ||||||
chr8:65625887
|
C | CT | 7 | a0001c0001t0001g0108a0001c0001t0017g0299a0001c0002t0002g0055others(4): Show | 7 | HG02135.hp1 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+1328dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625887 | ||||||
chr8:65625887
|
CT | C | 8 | a0001c0001t0001g0114a0001c0001t0003g0187a0001c0001t0003g0215others(5): Show | 8 | HG02486.hp1 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+1328delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625887 | ||||||
chr8:65625910
|
C | T | 1 | a0001c0001t0005g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.183+1306G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625910 | ||||||
chr8:65625918
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.183+1298G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625918 | ||||||
chr8:65625919
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+1297T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625919 | ||||||
chr8:65625988
|
A | C | 13 | a0001c0002t0002g0004a0001c0002t0002g0013a0001c0002t0002g0050others(10): Show | 17 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+1228T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625988 | ||||||
chr8:65626009
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.183+1207G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626009 | ||||||
chr8:65626357
|
A | C | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+859T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626357 | ||||||
chr8:65626417
|
A | C | 1 | a0001c0002t0002g0064 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.183+799T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626417 | ||||||
chr8:65626433
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+783T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626433 | ||||||
chr8:65626441
|
T | TA | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.183+774dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626441 | ||||||
chr8:65626441
|
T | TAA | 32 | a0001c0001t0001g0108a0001c0001t0003g0009a0001c0001t0003g0023others(29): Show | 37 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+773_183+774dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626441 | ||||||
chr8:65626479
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+737T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626479 | ||||||
chr8:65626740
|
G | A | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+476C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626740 | ||||||
chr8:65626921
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 186 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.183+295G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626921 | ||||||
chr8:65626921
|
C | T | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(13): Show | 18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+295G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626921 | ||||||
chr8:65626977
|
C | T | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0181others(13): Show | 18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+239G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626977 | ||||||
chr8:65627002
|
CA | C | 74 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(71): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.183+213delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65627002 | ||||||
chr8:65627023
|
TA | T | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.183+192delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65627023 | ||||||
chr8:65627435
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG00621.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-35-2A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627435 | ||||||
chr8:65627444
|
G | A | 8 | a0001c0001t0003g0009a0001c0001t0003g0221a0001c0001t0003g0222others(5): Show | 10 | HG01070.hp1 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-11C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627444 | ||||||
chr8:65627449
|
G | T | 1 | a0001c0001t0023g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-35-16C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627449 | ||||||
chr8:65627556
|
C | T | 1 | a0001c0003t0004g0289 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-35-123G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627556 | ||||||
chr8:65627563
|
AT | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-35-131delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627563 | ||||||
chr8:65627576
|
CAGTTTGA others(4): Show |
C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-35-154_-35-144del others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627576 | ||||||
chr8:65627660
|
T | G | 1 | a0001c0001t0005g0315 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-35-227A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627660 | ||||||
chr8:65627670
|
TTA | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | HG01175.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-35-239_-35-238del others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627670 | ||||||
chr8:65627672
|
A | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(159): Show | 198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-35-239T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627672 | ||||||
chr8:65627683
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-250G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627683 | ||||||
chr8:65627818
|
G | A | 1 | a0001c0002t0002g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-35-385C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627818 | ||||||
chr8:65627821
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-35-388C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627821 | ||||||
chr8:65628071
|
G | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0237a0001c0001t0003g0240others(1): Show | 5 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-638C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628071 | ||||||
chr8:65628204
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-35-771T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628204 | ||||||
chr8:65628238
|
T | C | 1 | a0001c0002t0004g0280 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-35-805A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628238 | ||||||
chr8:65628247
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-814A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628247 | ||||||
chr8:65628386
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-35-953C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628386 | ||||||
chr8:65628391
|
A | AT | 40 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0003g0186others(37): Show | 44 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35-959dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | ||||||
chr8:65628391
|
A | ATT | 35 | a0001c0001t0010g0281a0001c0001t0020g0282a0001c0002t0002g0050others(32): Show | 37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-35-960_-35-959dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | ||||||
chr8:65628391
|
A | ATTT | 8 | a0001c0002t0004g0253a0001c0002t0004g0254a0001c0002t0004g0255others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35-961_-35-959dup others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | ||||||
chr8:65628391
|
AT | A | 65 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0115others(62): Show | 75 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-35-959delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | ||||||
chr8:65628391
|
ATT | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-35-960_-35-959del others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | ||||||
chr8:65628656
|
G | A | 18 | a0001c0001t0003g0009a0001c0001t0003g0023a0001c0001t0003g0182others(15): Show | 21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35-1223C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628656 | ||||||
chr8:65628801
|
G | A | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35-1368C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628801 | ||||||
chr8:65628843
|
A | C | 1 | a0001c0001t0003g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-35-1410T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628843 | ||||||
chr8:65628853
|
C | CA | 163 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 199 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.-35-1421dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628853 | ||||||
chr8:65628865
|
G | A | 1 | a0001c0001t0018g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-35-1432C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628865 | ||||||
chr8:65628949
|
T | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1516A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628949 | ||||||
chr8:65628953
|
A | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1520T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628953 | ||||||
chr8:65628956
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1523G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628956 | ||||||
chr8:65628963
|
G | C | 1 | a0001c0003t0004g0297 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35-1530C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628963 | ||||||
chr8:65629146
|
C | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35-1713G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629146 | ||||||
chr8:65629154
|
C | CA | 6 | a0001c0001t0001g0022a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 7 | HG00140.hp1 HG02257.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35-1722dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629154 | ||||||
chr8:65629328
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-1895T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629328 | ||||||
chr8:65629401
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-35-1968T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629401 | ||||||
chr8:65629555
|
C | G | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2122G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629555 | ||||||
chr8:65629556
|
T | G | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2123A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629556 | ||||||
chr8:65629557
|
T | C | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2124A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629557 | ||||||
chr8:65629558
|
T | A | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2125A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629558 | ||||||
chr8:65629577
|
G | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2144C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629577 | ||||||
chr8:65629782
|
G | C | 1 | a0001c0001t0003g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-35-2349C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629782 | ||||||
chr8:65629798
|
C | CA | 16 | a0001c0001t0005g0310a0001c0001t0005g0311a0001c0001t0005g0312others(13): Show | 17 | HG00738.hp1 HG01069.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35-2366dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | ||||||
chr8:65629798
|
CA | C | 14 | a0001c0001t0001g0118a0001c0001t0006g0034a0001c0001t0006g0035others(11): Show | 14 | HG00642.hp2 HG02027.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-35-2366delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | ||||||
chr8:65629798
|
CAA | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(158): Show | 197 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.-35-2367_-35-2366d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | ||||||
chr8:65629816
|
A | C | 16 | a0001c0003t0004g0011a0001c0003t0004g0285a0001c0003t0004g0287others(13): Show | 19 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-35-2383T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629816 | ||||||
chr8:65629819
|
T | A | 1 | a0001c0002t0002g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-35-2386A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629819 | ||||||
chr8:65629842
|
G | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-35-2409C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629842 | ||||||
chr8:65629916
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2483C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629916 | ||||||
chr8:65629999
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-35-2566C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629999 | ||||||
chr8:65630042
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2609C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630042 | ||||||
chr8:65630202
|
T | C | 9 | a0001c0002t0004g0272a0001c0002t0004g0273a0001c0002t0004g0274others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35-2769A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630202 | ||||||
chr8:65630218
|
GAT | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-35-2787_-35-2786d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630218 | ||||||
chr8:65630504
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-3071A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630504 | ||||||
chr8:65630509
|
A | C | 3 | a0001c0001t0006g0035a0001c0001t0006g0037a0001c0001t0015g0036 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-35-3076T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630509 | ||||||
chr8:65630536
|
C | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 99 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-35-3103G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630536 | ||||||
chr8:65630817
|
T | TAA | 161 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(158): Show | 196 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.-36+3179_-36+3180d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630817 | ||||||
chr8:65630829
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+3169A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630829 | ||||||
chr8:65630940
|
T | TCCACAGG others(4): Show |
1 | a0001c0002t0002g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36+3047_-36+3057d others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630940 | ||||||
chr8:65630941
|
C | A | 9 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0037others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+3057G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630941 | ||||||
chr8:65631051
|
G | A | 1 | a0001c0001t0010g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-36+2947C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631051 | ||||||
chr8:65631099
|
G | A | 1 | a0001c0001t0005g0315 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-36+2899C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631099 | ||||||
chr8:65631246
|
T | C | 20 | a0001c0001t0005g0033a0001c0001t0005g0300a0001c0001t0005g0301others(17): Show | 21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36+2752A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631246 | ||||||
chr8:65631290
|
C | T | 2 | a0001c0001t0003g0248a0001c0001t0003g0249 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+2708G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631290 | ||||||
chr8:65631303
|
C | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2695G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631303 | ||||||
chr8:65631334
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-36+2664T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631334 | ||||||
chr8:65631381
|
C | T | 1 | a0003c0005t0002g0047 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-36+2617G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631381 | ||||||
chr8:65631423
|
G | A | 6 | a0001c0001t0003g0010a0001c0001t0003g0232a0001c0001t0003g0233others(3): Show | 8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-36+2575C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631423 | ||||||
chr8:65631434
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2564C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631434 | ||||||
chr8:65631525
|
C | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 105 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-36+2473G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631525 | ||||||
chr8:65631541
|
G | T | 1 | a0001c0002t0002g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-36+2457C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631541 | ||||||
chr8:65631742
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2256G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631742 | ||||||
chr8:65631743
|
G | A | 9 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0238others(6): Show | 11 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36+2255C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631743 | ||||||
chr8:65631883
|
TA | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 213 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.-36+2114delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631883 | ||||||
chr8:65631883
|
TAA | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG02965.hp1 NA18939.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36+2113_-36+2114d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631883 | ||||||
chr8:65631908
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-36+2090A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631908 | ||||||
chr8:65631915
|
G | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-36+2083C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631915 | ||||||
chr8:65631939
|
ATAT | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2056_-36+2058d others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631939 | ||||||
chr8:65632122
|
T | C | 1 | a0001c0001t0003g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36+1876A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632122 | ||||||
chr8:65632167
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-36+1831G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632167 | ||||||
chr8:65632208
|
G | C | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-36+1790C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632208 | ||||||
chr8:65632270
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-36+1728G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632270 | ||||||
chr8:65632507
|
G | T | 3 | a0001c0001t0010g0281a0001c0001t0010g0283a0001c0001t0020g0282 | 3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-36+1491C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632507 | ||||||
chr8:65632554
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-36+1444T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632554 | ||||||
chr8:65632570
|
G | A | 1 | a0001c0001t0018g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-36+1428C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632570 | ||||||
chr8:65632825
|
CA | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-36+1172delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632825 | ||||||
chr8:65633319
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-36+679T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633319 | ||||||
chr8:65633462
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-36+536T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633462 | ||||||
chr8:65633484
|
G | A | 1 | a0001c0002t0002g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-36+514C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633484 | ||||||
chr8:65633546
|
C | G | 34 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0251others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.-36+452G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633546 | ||||||
chr8:65633554
|
G | A | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-36+444C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633554 | ||||||
chr8:65633834
|
G | A | 2 | a0001c0001t0003g0248a0001c0001t0003g0249 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+164C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633834 | ||||||
chr8:65633891
|
C | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+107G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633891 | ||||||
chr8:65633895
|
C | A | 1 | a0001c0002t0004g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-36+103G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633895 | ||||||
chr8:65633913
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-36+85G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633913 | ||||||
chr8:65633937
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-36+61C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633937 |