geneid | 64756 |
---|---|
ensemblid | ENSG00000123472.13 |
hgncid | 18803 |
symbol | ATPAF1 |
name | ATP synthase mitochondrial F1 complex assembly factor 1 |
refseq_nuc | NM_001394565.1 |
refseq_prot | NP_001381494.1 |
ensembl_nuc | ENST00000574428.6 |
ensembl_prot | ENSP00000459167.2 |
mane_status | MANE Select |
chr | chr1 |
start | 46632737 |
end | 46668364 |
strand | - |
ver | v1.2 |
region | chr1:46632737-46668364 |
region5000 | chr1:46627737-46673364 |
regionname0 | ATPAF1_chr1_46632737_46668364 |
regionname5000 | ATPAF1_chr1_46627737_46673364 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 328 | 359 | 85 | 51 | 183 | 8 | 32 | 142 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002 | 1/1 | 328 | 51 | 9 | 7 | 15 | 4 | 14 | 10 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0003 | 0/0 | 328 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 987 | 358 | 84 | 51 | 183 | 8 | 32 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
c0002 | 1/1 | 987 | 51 | 9 | 7 | 15 | 4 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
c0003 | 0/0 | 987 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
c0004 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3082 | 111 | 34 | 4 | 63 | 0 | 9 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0002 | 0/0 | 3082 | 108 | 10 | 22 | 64 | 1 | 11 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0003 | 0/0 | 3083 | 75 | 12 | 21 | 31 | 4 | 7 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0004 | 0/1 | 3083 | 52 | 18 | 7 | 9 | 3 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0005 | 0/0 | 3082 | 15 | 0 | 2 | 11 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0006 | 0/0 | 3082 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0007 | 0/0 | 3083 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0008 | 0/0 | 3085 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0009 | 0/0 | 3082 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0010 | 0/0 | 3082 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0011 | 0/0 | 3082 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0012 | 0/0 | 3083 | 3 | 0 | 0 | 0 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0013 | 0/0 | 3082 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0014 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0015 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0016 | 0/0 | 3082 | 2 | 1 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0017 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0018 | 0/0 | 3083 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0019 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0020 | 0/0 | 3083 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0021 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0022 | 0/0 | 3082 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0023 | 0/0 | 3082 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0024 | 0/0 | 3082 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0025 | 0/0 | 3083 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0026 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0027 | 0/0 | 3083 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0028 | 0/0 | 3083 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0029 | 0/0 | 3082 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
t0030 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 2 | 1 | 18 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0002 | 0/0 | 18 | 1 | 7 | 7 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0003 | 0/0 | 16 | 1 | 9 | 3 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0004 | 0/0 | 14 | 0 | 4 | 8 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0006 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 987 | 358 | 84 | 51 | 183 | 8 | 32 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0004 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002 | 1/1 | 987 | 51 | 9 | 7 | 15 | 4 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0003c0003 | 0/0 | 987 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4068 | 110 | 34 | 4 | 63 | 0 | 9 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0002 | 0/0 | 4068 | 105 | 9 | 20 | 64 | 1 | 11 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0003 | 0/0 | 4069 | 75 | 12 | 21 | 31 | 4 | 7 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0004 | 0/0 | 4069 | 10 | 9 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0005 | 0/0 | 4068 | 15 | 0 | 2 | 11 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0006 | 0/0 | 4068 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0008 | 0/0 | 4071 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0009 | 0/0 | 4068 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0010 | 0/0 | 4068 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0011 | 0/0 | 4068 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0012 | 0/0 | 4069 | 3 | 0 | 0 | 0 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0013 | 0/0 | 4068 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0014 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0015 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0016 | 0/0 | 4068 | 2 | 1 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0017 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0018 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0019 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0020 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0021 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0022 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0023 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0024 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0026 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0028 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0029 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0001t0030 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0001c0004t0002 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002t0001 | 1/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002t0004 | 0/1 | 4069 | 42 | 9 | 6 | 9 | 3 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002t0007 | 0/0 | 4069 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002t0025 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0002c0002t0027 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
a0003c0003t0002 | 0/0 | 4068 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | copy fasta | chr1 | 46627737 | 46673364 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 2 | 1 | 18 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0002 | 0/0 | 18 | 1 | 7 | 7 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0004 | 0/0 | 14 | 0 | 4 | 8 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0003 | 0/0 | 16 | 1 | 9 | 3 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0006 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0006g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0006g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0008g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0011g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0012g0050 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0012g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0013g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0015g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0016g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0016g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0018g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0021g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0022g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0023g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0024g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0026g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0028g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0029g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0001t0030g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0001c0004t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0004g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0007g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0007g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0025g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0002c0002t0027g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
a0003c0003t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0004 | g0086 | EUR | GBR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00280 | hp1 | a0001 | c0001 | t0013 | g0038 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0098 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00323 | hp1 | a0002 | c0002 | t0027 | g0070 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00323 | hp2 | a0002 | c0002 | t0004 | g0082 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00438 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0051 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00597 | hp2 | a0002 | c0002 | t0007 | g0024 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00642 | hp1 | a0001 | c0001 | t0016 | g0188 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00673 | hp1 | a0001 | c0001 | t0019 | g0148 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01069 | hp1 | a0001 | c0001 | t0022 | g0202 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01070 | hp2 | a0003 | c0003 | t0002 | g0046 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0046 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01243 | hp2 | a0002 | c0002 | t0004 | g0063 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01256 | hp2 | a0002 | c0002 | t0025 | g0083 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01257 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01358 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0120 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01515 | hp2 | a0001 | c0001 | t0012 | g0050 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01517 | hp2 | a0001 | c0001 | t0012 | g0050 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0025 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0067 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01952 | hp1 | a0001 | c0001 | t0029 | g0200 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01981 | hp2 | a0002 | c0002 | t0004 | g0062 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02027 | hp1 | a0002 | c0002 | t0007 | g0023 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0231 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0074 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0248 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02280 | hp2 | a0001 | c0004 | t0002 | g0207 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0060 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02602 | hp1 | a0002 | c0002 | t0004 | g0076 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02615 | hp1 | a0001 | c0001 | t0026 | g0132 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02683 | hp1 | a0002 | c0002 | t0004 | g0010 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02698 | hp2 | a0002 | c0002 | t0004 | g0084 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02723 | hp2 | a0002 | c0002 | t0004 | g0056 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02735 | hp1 | a0002 | c0002 | t0004 | g0078 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0061 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02896 | hp2 | a0002 | c0002 | t0004 | g0066 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02922 | hp2 | a0001 | c0001 | t0017 | g0142 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02965 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02970 | hp2 | a0002 | c0002 | t0004 | g0064 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0196 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0247 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03017 | hp1 | a0002 | c0002 | t0004 | g0072 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03139 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03195 | hp1 | a0001 | c0001 | t0016 | g0187 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03490 | hp1 | a0001 | c0001 | t0024 | g0205 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03491 | hp1 | a0002 | c0002 | t0004 | g0007 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03516 | hp2 | a0002 | c0002 | t0004 | g0025 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0195 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03704 | hp1 | a0002 | c0002 | t0004 | g0077 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0057 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03710 | hp1 | a0002 | c0002 | t0004 | g0010 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03834 | hp2 | a0002 | c0002 | t0004 | g0010 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03942 | hp1 | a0001 | c0001 | t0012 | g0109 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03942 | hp2 | a0002 | c0002 | t0004 | g0068 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0232 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04199 | hp2 | a0002 | c0002 | t0004 | g0073 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04204 | hp1 | a0002 | c0002 | t0004 | g0058 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG04228 | hp2 | a0002 | c0002 | t0004 | g0079 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18747 | hp1 | a0002 | c0002 | t0007 | g0024 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18906 | hp2 | a0001 | c0001 | t0030 | g0197 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18939 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18946 | hp2 | a0002 | c0002 | t0007 | g0071 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18947 | hp2 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18961 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18967 | hp2 | a0001 | c0001 | t0028 | g0110 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18971 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18988 | hp2 | a0002 | c0002 | t0007 | g0023 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0075 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18997 | hp2 | a0001 | c0001 | t0018 | g0161 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18998 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19005 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19006 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19006 | hp2 | a0002 | c0002 | t0007 | g0081 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19010 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0243 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0145 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19054 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19055 | hp2 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19056 | hp2 | a0001 | c0001 | t0013 | g0038 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19087 | hp1 | a0001 | c0001 | t0021 | g0241 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA20805 | hp2 | a0002 | c0002 | t0004 | g0085 | EUR | TSI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0069 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA21309 | hp1 | a0002 | c0002 | t0004 | g0055 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
NA21309 | hp2 | a0001 | c0001 | t0020 | g0130 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0004 | g0087 | REF | REF | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0065 | REF | REF | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46635868
|
T | G | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.895A>C | p.Asn299His | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 937/4068 | 895/987 | 299/328 | chr1 | 46635868 | ||
chr1:46668139
|
T | C | 2 | a0001a0003 | 361 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(358): Show |
missense_variant | MODERATE | c.184A>G | p.Ser62Gly | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/9 | 226/4068 | 184/987 | 62/328 | chr1 | 46668139 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46635884
|
G | C | 1 | a0001c0004 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.879C>G | p.Thr293Thr | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 921/4068 | 879/987 | 293/328 | chr1 | 46635884 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46632819
|
G | A | 1 | a0002c0002t0027 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2957 | chr1 | 46632819 | |||||
chr1:46632997
|
T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2779A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2779 | chr1 | 46632997 | |||||
chr1:46632999
|
C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2777 | chr1 | 46632999 | |||||
chr1:46633151
|
C | T | 1 | a0001c0001t0012 | 3 | HG01515.hp2 HG01517.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2625G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2625 | chr1 | 46633151 | |||||
chr1:46633238
|
G | A | 1 | a0001c0001t0016 | 2 | HG00642.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2538C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2538 | chr1 | 46633238 | |||||
chr1:46633418
|
G | GA | 10 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(7): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2357dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2357 | chr1 | 46633418 | |||||
chr1:46633426
|
A | C | 2 | a0001c0001t0009a0001c0001t0014 | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2350T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2350 | chr1 | 46633426 | |||||
chr1:46633487
|
C | T | 2 | a0001c0001t0009a0001c0001t0014 | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2289G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2289 | chr1 | 46633487 | |||||
chr1:46633498
|
A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2278 | chr1 | 46633498 | |||||
chr1:46633499
|
C | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2277G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2277 | chr1 | 46633499 | |||||
chr1:46633525
|
G | A | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2251 | chr1 | 46633525 | |||||
chr1:46633563
|
A | C | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(3): Show | 84 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2213T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2213 | chr1 | 46633563 | |||||
chr1:46633674
|
C | A | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*2102G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2102 | chr1 | 46633674 | |||||
chr1:46633792
|
T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1984 | chr1 | 46633792 | |||||
chr1:46633794
|
T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1982 | chr1 | 46633794 | |||||
chr1:46633797
|
A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1979T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1979 | chr1 | 46633797 | |||||
chr1:46633801
|
A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1975 | chr1 | 46633801 | |||||
chr1:46633802
|
C | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1974G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1974 | chr1 | 46633802 | |||||
chr1:46633803
|
T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1973 | chr1 | 46633803 | |||||
chr1:46633805
|
T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1971 | chr1 | 46633805 | |||||
chr1:46633806
|
G | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1970 | chr1 | 46633806 | |||||
chr1:46633807
|
T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1969 | chr1 | 46633807 | |||||
chr1:46633810
|
G | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1966C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1966 | chr1 | 46633810 | |||||
chr1:46633811
|
G | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1965 | chr1 | 46633811 | |||||
chr1:46633814
|
A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1962T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1962 | chr1 | 46633814 | |||||
chr1:46633817
|
A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1959T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1959 | chr1 | 46633817 | |||||
chr1:46633818
|
A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1958T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1958 | chr1 | 46633818 | |||||
chr1:46633819
|
C | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1957G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1957 | chr1 | 46633819 | |||||
chr1:46633831
|
G | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1945C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1945 | chr1 | 46633831 | |||||
chr1:46633835
|
A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1941T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1941 | chr1 | 46633835 | |||||
chr1:46633837
|
A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1939T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1939 | chr1 | 46633837 | |||||
chr1:46633843
|
A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1933T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1933 | chr1 | 46633843 | |||||
chr1:46633851
|
C | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1925 | chr1 | 46633851 | |||||
chr1:46633852
|
T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1924 | chr1 | 46633852 | |||||
chr1:46633856
|
T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1920 | chr1 | 46633856 | |||||
chr1:46633894
|
T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1882 | chr1 | 46633894 | |||||
chr1:46633897
|
G | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1879C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1879 | chr1 | 46633897 | |||||
chr1:46633898
|
A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1878 | chr1 | 46633898 | |||||
chr1:46634049
|
T | C | 11 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(8): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1727A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1727 | chr1 | 46634049 | |||||
chr1:46634255
|
C | T | 1 | a0001c0001t0013 | 2 | HG00280.hp1 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1521G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1521 | chr1 | 46634255 | |||||
chr1:46634377
|
C | T | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1399 | chr1 | 46634377 | |||||
chr1:46634403
|
G | A | 1 | a0001c0001t0019 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1373 | chr1 | 46634403 | |||||
chr1:46634410
|
G | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1366C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1366 | chr1 | 46634410 | |||||
chr1:46634427
|
C | A | 4 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(1): Show | 82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1349 | chr1 | 46634427 | |||||
chr1:46634487
|
C | T | 10 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(7): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1289 | chr1 | 46634487 | |||||
chr1:46634654
|
G | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1122 | chr1 | 46634654 | |||||
chr1:46634665
|
C | T | 1 | a0001c0001t0022 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1111G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1111 | chr1 | 46634665 | |||||
chr1:46634704
|
C | A | 1 | a0001c0001t0014 | 2 | HG02965.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1072G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1072 | chr1 | 46634704 | |||||
chr1:46634818
|
T | G | 1 | a0002c0002t0007 | 6 | HG00597.hp2 HG02027.hp1 NA18747.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*958A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 958 | chr1 | 46634818 | |||||
chr1:46634911
|
T | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*865A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 865 | chr1 | 46634911 | |||||
chr1:46634956
|
C | T | 1 | a0001c0001t0021 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 820 | chr1 | 46634956 | |||||
chr1:46635128
|
C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 648 | chr1 | 46635128 | |||||
chr1:46635186
|
T | C | 1 | a0001c0001t0005 | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 590 | chr1 | 46635186 | |||||
chr1:46635299
|
T | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*477A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 477 | chr1 | 46635299 | |||||
chr1:46635343
|
C | A | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 433 | chr1 | 46635343 | |||||
chr1:46635501
|
G | C | 1 | a0001c0001t0029 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 275 | chr1 | 46635501 | |||||
chr1:46635692
|
T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 84 | chr1 | 46635692 | |||||
chr1:46668333
|
G | GCCT | 1 | a0001c0001t0008 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12dupAGG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/9 | 12 | chr1 | 46668333 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46636075
|
C | T | 1 | a0002c0002t0004g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.793-105G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636075 | ||||||
chr1:46636124
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793-154G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636124 | ||||||
chr1:46636386
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(244): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.793-416G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636386 | ||||||
chr1:46636731
|
T | TA | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-762dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636731 | ||||||
chr1:46636859
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-889T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636859 | ||||||
chr1:46636890
|
G | A | 1 | a0001c0001t0014g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.793-920C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636890 | ||||||
chr1:46636927
|
T | C | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793-957A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636927 | ||||||
chr1:46637027
|
C | T | 1 | a0001c0001t0002g0048 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.793-1057G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637027 | ||||||
chr1:46637140
|
G | C | 1 | a0001c0001t0003g0093 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.793-1170C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637140 | ||||||
chr1:46637284
|
A | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.793-1314T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637284 | ||||||
chr1:46637293
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.793-1323A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637293 | ||||||
chr1:46637423
|
C | T | 2 | a0001c0001t0010g0243a0001c0001t0030g0197 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.793-1453G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637423 | ||||||
chr1:46637483
|
C | G | 2 | a0001c0001t0010g0195a0001c0001t0010g0196 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.793-1513G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637483 | ||||||
chr1:46637500
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.793-1530G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637500 | ||||||
chr1:46637517
|
C | T | 1 | a0002c0002t0004g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793-1547G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637517 | ||||||
chr1:46637743
|
T | C | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-1773A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637743 | ||||||
chr1:46637945
|
T | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.793-1975A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637945 | ||||||
chr1:46638082
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(49): Show | 95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.793-2112G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638082 | ||||||
chr1:46638120
|
A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-2150T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638120 | ||||||
chr1:46638151
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.793-2181C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638151 | ||||||
chr1:46638159
|
T | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.793-2189A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638159 | ||||||
chr1:46638198
|
A | T | 66 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(63): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.793-2228T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638198 | ||||||
chr1:46638214
|
C | A | 29 | a0002c0002t0004g0007a0002c0002t0004g0010a0002c0002t0004g0057others(26): Show | 40 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.793-2244G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638214 | ||||||
chr1:46638219
|
T | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.793-2249A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638219 | ||||||
chr1:46638400
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.793-2430A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638400 | ||||||
chr1:46638479
|
G | C | 1 | a0002c0002t0004g0084 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.793-2509C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638479 | ||||||
chr1:46638488
|
G | T | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793-2518C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638488 | ||||||
chr1:46638621
|
CA | C | 167 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0002others(164): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.793-2652delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638621 | ||||||
chr1:46638658
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-2688G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638658 | ||||||
chr1:46638659
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(241): Show | 403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.793-2689T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638659 | ||||||
chr1:46638700
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(49): Show | 95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.793-2730T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638700 | ||||||
chr1:46638718
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.793-2748A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638718 | ||||||
chr1:46638798
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793-2828G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638798 | ||||||
chr1:46638828
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.793-2858G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638828 | ||||||
chr1:46638912
|
G | A | 1 | a0001c0001t0030g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793-2942C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638912 | ||||||
chr1:46638949
|
T | C | 1 | a0002c0002t0004g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.793-2979A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638949 | ||||||
chr1:46639036
|
T | C | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.793-3066A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639036 | ||||||
chr1:46639112
|
A | C | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.793-3142T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639112 | ||||||
chr1:46639235
|
T | TAC | 73 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(70): Show | 135 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.793-3267_793-3266d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639235 | ||||||
chr1:46639235
|
T | TACAC | 96 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(93): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.793-3269_793-3266d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639235 | ||||||
chr1:46639328
|
G | A | 39 | a0001c0001t0004g0129a0002c0002t0004g0007a0002c0002t0004g0010others(36): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.793-3358C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639328 | ||||||
chr1:46639412
|
C | A | 1 | a0001c0001t0030g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793-3442G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639412 | ||||||
chr1:46639487
|
T | A | 1 | a0001c0001t0005g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.793-3517A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639487 | ||||||
chr1:46639553
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.793-3583C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639553 | ||||||
chr1:46639616
|
C | T | 1 | a0002c0002t0004g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.792+3578G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639616 | ||||||
chr1:46639697
|
T | A | 3 | a0001c0001t0002g0199a0001c0001t0002g0201a0001c0001t0029g0200 | 3 | HG00639.hp1 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.792+3497A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639697 | ||||||
chr1:46639790
|
A | G | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.792+3404T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639790 | ||||||
chr1:46639807
|
A | G | 11 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+3387T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639807 | ||||||
chr1:46639945
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(244): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.792+3249A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639945 | ||||||
chr1:46640278
|
G | A | 87 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(84): Show | 131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.792+2916C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640278 | ||||||
chr1:46640386
|
G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+2808C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640386 | ||||||
chr1:46640427
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0015g0247a0001c0001t0015g0248others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+2767A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640427 | ||||||
chr1:46640627
|
C | CT | 2 | a0001c0001t0004g0031a0001c0001t0004g0131 | 3 | HG02559.hp1 HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.792+2566dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640627 | ||||||
chr1:46640635
|
A | AAAAC | 92 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(89): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.792+2555_792+2558d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640635 | ||||||
chr1:46640635
|
A | AAAACAAA others(1): Show |
3 | a0001c0001t0003g0106a0001c0001t0003g0107a0002c0002t0004g0069 | 3 | HG01123.hp1 HG03239.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.792+2551_792+2558d others(10): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640635 | ||||||
chr1:46640683
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.792+2511A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640683 | ||||||
chr1:46640948
|
T | C | 1 | a0001c0001t0010g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.792+2246A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640948 | ||||||
chr1:46641253
|
A | AT | 29 | a0002c0002t0004g0007a0002c0002t0004g0010a0002c0002t0004g0057others(26): Show | 40 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.792+1940dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641253 | ||||||
chr1:46641277
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(241): Show | 403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.792+1917A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641277 | ||||||
chr1:46641344
|
G | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.792+1850C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641344 | ||||||
chr1:46641370
|
T | TG | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.792+1823_792+1824i others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641370 | ||||||
chr1:46641442
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.792+1752G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641442 | ||||||
chr1:46641451
|
G | A | 1 | a0001c0001t0002g0048 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.792+1743C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641451 | ||||||
chr1:46641505
|
C | G | 2 | a0001c0001t0010g0195a0001c0001t0010g0196 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.792+1689G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641505 | ||||||
chr1:46641535
|
C | T | 3 | a0001c0001t0003g0128a0002c0002t0004g0074a0002c0002t0004g0075 | 3 | HG02074.hp2 HG02622.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.792+1659G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641535 | ||||||
chr1:46641537
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.792+1657C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641537 | ||||||
chr1:46641539
|
G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+1655C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641539 | ||||||
chr1:46641647
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.792+1547A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641647 | ||||||
chr1:46641718
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.792+1476T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641718 | ||||||
chr1:46641877
|
TG | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0181a0001c0001t0001g0184 | 5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+1316delC | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641877 | ||||||
chr1:46642074
|
G | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1120C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642074 | ||||||
chr1:46642317
|
A | G | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.792+877T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642317 | ||||||
chr1:46642460
|
C | A | 5 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(2): Show | 5 | HG01256.hp1 HG01515.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+734G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642460 | ||||||
chr1:46642535
|
A | T | 1 | a0001c0001t0014g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.792+659T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642535 | ||||||
chr1:46642671
|
A | G | 95 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(92): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.792+523T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642671 | ||||||
chr1:46642693
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.792+501C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642693 | ||||||
chr1:46642786
|
TAAC | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+405_792+407del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642786 | ||||||
chr1:46642821
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.792+373A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642821 | ||||||
chr1:46642874
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.792+320A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642874 | ||||||
chr1:46642961
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+233G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642961 | ||||||
chr1:46642962
|
A | C | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+232T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642962 | ||||||
chr1:46642963
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+231A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642963 | ||||||
chr1:46643030
|
A | C | 1 | a0001c0001t0003g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.792+164T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643030 | ||||||
chr1:46643031
|
T | C | 1 | a0001c0001t0001g0014 | 4 | NA18612.hp2 NA18963.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+163A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643031 | ||||||
chr1:46643041
|
T | C | 1 | a0002c0002t0004g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.792+153A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643041 | ||||||
chr1:46643156
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.792+38A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643156 | ||||||
chr1:46643157
|
G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+37C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643157 | ||||||
chr1:46643348
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-47G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643348 | ||||||
chr1:46643417
|
A | G | 95 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(92): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.685-116T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643417 | ||||||
chr1:46643579
|
A | G | 180 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(177): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.685-278T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643579 | ||||||
chr1:46643656
|
C | T | 192 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0135others(189): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.685-355G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643656 | ||||||
chr1:46643801
|
G | A | 67 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(64): Show | 123 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.685-500C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643801 | ||||||
chr1:46643812
|
G | C | 1 | a0001c0001t0003g0112 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.685-511C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643812 | ||||||
chr1:46643838
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0181a0001c0001t0001g0184 | 5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-537T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643838 | ||||||
chr1:46644072
|
A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-771T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644072 | ||||||
chr1:46644126
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.685-825A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644126 | ||||||
chr1:46644156
|
A | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(176): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.685-855T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644156 | ||||||
chr1:46644158
|
G | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(176): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.685-857C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644158 | ||||||
chr1:46644220
|
T | C | 1 | a0002c0002t0004g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.685-919A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644220 | ||||||
chr1:46644244
|
T | C | 95 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(92): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.684+917A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644244 | ||||||
chr1:46644311
|
T | TG | 191 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0136others(188): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.684+849_684+850ins others(1): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644311 | ||||||
chr1:46644466
|
G | A | 1 | a0002c0002t0004g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684+695C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644466 | ||||||
chr1:46644559
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.684+602C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644559 | ||||||
chr1:46644565
|
G | GT | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(68): Show | 127 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.684+595dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644565 | ||||||
chr1:46644624
|
ATT | A | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+535_684+536del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644624 | ||||||
chr1:46644742
|
C | CATTT | 244 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(241): Show | 403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.684+418_684+419ins others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644742 | ||||||
chr1:46644838
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.684+323G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644838 | ||||||
chr1:46644996
|
G | C | 95 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(92): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.684+165C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644996 | ||||||
chr1:46645040
|
C | T | 95 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(92): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.684+121G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645040 | ||||||
chr1:46645079
|
T | C | 2 | a0001c0001t0004g0031a0001c0001t0004g0131 | 3 | HG02559.hp1 HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.684+82A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645079 | ||||||
chr1:46645094
|
G | GC | 174 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(171): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.684+66dupG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645094 | ||||||
chr1:46645136
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.684+25A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645136 | ||||||
chr1:46645365
|
TA | T | 3 | a0001c0001t0009g0034a0001c0001t0014g0144a0001c0001t0014g0145 | 4 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-110delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645365 | ||||||
chr1:46645501
|
C | T | 1 | a0002c0002t0004g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.589-245G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645501 | ||||||
chr1:46645590
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0214 | 2 | NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.589-334G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645590 | ||||||
chr1:46645591
|
G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-335C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645591 | ||||||
chr1:46645634
|
A | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0203a0001c0001t0002g0212others(1): Show | 5 | HG00099.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-378T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645634 | ||||||
chr1:46645753
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-497A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645753 | ||||||
chr1:46645804
|
T | C | 1 | a0002c0002t0004g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.589-548A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645804 | ||||||
chr1:46645946
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0017others(38): Show | 74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.589-690G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645946 | ||||||
chr1:46645998
|
G | C | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-742C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645998 | ||||||
chr1:46646078
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.589-822C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646078 | ||||||
chr1:46646151
|
A | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-895T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646151 | ||||||
chr1:46646205
|
TG | T | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-950delC | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646205 | ||||||
chr1:46646314
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.589-1058A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646314 | ||||||
chr1:46646400
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.589-1144T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646400 | ||||||
chr1:46646413
|
C | T | 1 | a0002c0002t0004g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.589-1157G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646413 | ||||||
chr1:46646435
|
C | CTGATA | 3 | a0001c0001t0003g0124a0001c0001t0003g0125a0002c0002t0004g0066 | 3 | HG02896.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.589-1184_589-1180d others(7): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646435 | ||||||
chr1:46646467
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.589-1211G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646467 | ||||||
chr1:46646523
|
G | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(49): Show | 95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-1267C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646523 | ||||||
chr1:46646845
|
A | C | 1 | a0002c0002t0004g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.589-1589T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646845 | ||||||
chr1:46646877
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-1621T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646877 | ||||||
chr1:46646904
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.589-1648A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646904 | ||||||
chr1:46647182
|
G | C | 1 | a0001c0001t0002g0224 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.589-1926C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647182 | ||||||
chr1:46647188
|
A | C | 1 | a0001c0001t0003g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.589-1932T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647188 | ||||||
chr1:46647238
|
T | C | 67 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(64): Show | 123 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.589-1982A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647238 | ||||||
chr1:46647503
|
TAC | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(123): Show | 212 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.589-2249_589-2248d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647503 | ||||||
chr1:46647523
|
CAT | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2269_589-2268d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647523 | ||||||
chr1:46647587
|
A | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2331T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647587 | ||||||
chr1:46647610
|
C | T | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-2354G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647610 | ||||||
chr1:46647623
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.589-2367C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647623 | ||||||
chr1:46647870
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0163 | 2 | NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.589-2614C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647870 | ||||||
chr1:46647946
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.589-2690A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647946 | ||||||
chr1:46648239
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.589-2983C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648239 | ||||||
chr1:46648265
|
C | T | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-3009G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648265 | ||||||
chr1:46648339
|
G | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.589-3083C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648339 | ||||||
chr1:46648391
|
C | T | 2 | a0001c0001t0003g0121a0002c0002t0004g0085 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.589-3135G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648391 | ||||||
chr1:46648815
|
C | T | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.589-3559G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648815 | ||||||
chr1:46648873
|
C | T | 95 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(92): Show | 171 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.589-3617G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648873 | ||||||
chr1:46648893
|
C | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.589-3637G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648893 | ||||||
chr1:46648948
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0018g0161 | 2 | NA18988.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.588+3633G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648948 | ||||||
chr1:46649113
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+3468C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649113 | ||||||
chr1:46649140
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0214 | 2 | NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.588+3441G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649140 | ||||||
chr1:46649157
|
C | CA | 76 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0165others(73): Show | 130 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.588+3423dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | ||||||
chr1:46649157
|
C | CAA | 11 | a0001c0001t0002g0022a0001c0001t0002g0190a0001c0001t0002g0225others(8): Show | 20 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.588+3422_588+3423d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | ||||||
chr1:46649157
|
CA | C | 44 | a0001c0001t0001g0032a0001c0001t0003g0003a0001c0001t0003g0005others(41): Show | 76 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.588+3423delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | ||||||
chr1:46649191
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3390A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649191 | ||||||
chr1:46649193
|
A | G | 1 | a0001c0001t0005g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588+3388T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649193 | ||||||
chr1:46649214
|
A | G | 1 | a0001c0001t0005g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588+3367T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649214 | ||||||
chr1:46649272
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.588+3309A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649272 | ||||||
chr1:46649307
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+3274T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649307 | ||||||
chr1:46649313
|
A | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3268T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649313 | ||||||
chr1:46649342
|
CAT | C | 4 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0229others(1): Show | 6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+3237_588+3238d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649342 | ||||||
chr1:46649379
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3202G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649379 | ||||||
chr1:46649380
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.588+3201T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649380 | ||||||
chr1:46649542
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3039G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649542 | ||||||
chr1:46649830
|
G | A | 1 | a0001c0001t0009g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588+2751C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649830 | ||||||
chr1:46649868
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+2713C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649868 | ||||||
chr1:46650051
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0151others(3): Show | 10 | HG00597.hp1 HG02135.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+2530G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650051 | ||||||
chr1:46650363
|
G | GA | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(55): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.588+2217dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650363 | ||||||
chr1:46650363
|
G | GAA | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0135others(11): Show | 19 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.588+2216_588+2217d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650363 | ||||||
chr1:46650392
|
GGAGA | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0211 | 3 | NA18962.hp1 NA18970.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.588+2185_588+2188d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650392 | ||||||
chr1:46650456
|
AT | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+2124delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650456 | ||||||
chr1:46650465
|
T | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+2116A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650465 | ||||||
chr1:46650500
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.588+2081T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650500 | ||||||
chr1:46650602
|
C | T | 6 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(3): Show | 7 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+1979G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650602 | ||||||
chr1:46650603
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0141a0001c0001t0001g0143others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1978C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650603 | ||||||
chr1:46650643
|
T | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | HG02486.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588+1938A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650643 | ||||||
chr1:46650767
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+1814G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650767 | ||||||
chr1:46650810
|
T | TA | 17 | a0001c0001t0001g0032a0001c0001t0001g0138a0001c0001t0001g0167others(14): Show | 20 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.588+1770dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650810 | ||||||
chr1:46650885
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.588+1696A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650885 | ||||||
chr1:46650951
|
G | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.588+1630C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650951 | ||||||
chr1:46650996
|
T | G | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+1585A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650996 | ||||||
chr1:46651046
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.588+1535A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651046 | ||||||
chr1:46651156
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+1425G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651156 | ||||||
chr1:46651328
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(64): Show | 117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.588+1253G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651328 | ||||||
chr1:46651334
|
A | AT | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(49): Show | 95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.588+1246dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651334 | ||||||
chr1:46651341
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0041 | 4 | NA18951.hp1 NA19063.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1240T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651341 | ||||||
chr1:46651462
|
G | A | 1 | a0001c0001t0001g0016 | 4 | HG02486.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1119C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651462 | ||||||
chr1:46651512
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0216 | 5 | NA18979.hp2 NA18986.hp2 NA19076.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1069G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651512 | ||||||
chr1:46651581
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+1000A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651581 | ||||||
chr1:46651582
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+999A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651582 | ||||||
chr1:46651585
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+996T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651585 | ||||||
chr1:46651586
|
CAATGGTT others(45): Show |
C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+943_588+994del others(52): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651586 | ||||||
chr1:46651640
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+941A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651640 | ||||||
chr1:46651643
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+938T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651643 | ||||||
chr1:46651645
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+936T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651645 | ||||||
chr1:46651646
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+935A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651646 | ||||||
chr1:46651649
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+932A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651649 | ||||||
chr1:46651650
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.588+931G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651650 | ||||||
chr1:46651651
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+930A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651651 | ||||||
chr1:46651654
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+927T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651654 | ||||||
chr1:46651655
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+926C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651655 | ||||||
chr1:46651657
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+924T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651657 | ||||||
chr1:46651659
|
C | CCCCCCCC others(45): Show |
1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+921_588+922ins others(52): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651659 | ||||||
chr1:46651665
|
T | C | 1 | a0002c0002t0004g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.588+916A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651665 | ||||||
chr1:46651735
|
T | G | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.588+846A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651735 | ||||||
chr1:46651896
|
G | T | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+685C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651896 | ||||||
chr1:46652072
|
G | A | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+509C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652072 | ||||||
chr1:46652205
|
C | CA | 11 | a0001c0001t0003g0111a0001c0001t0004g0029a0001c0001t0004g0030others(8): Show | 14 | HG01109.hp2 HG01167.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+375dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | ||||||
chr1:46652205
|
CA | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(129): Show | 241 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(238): Show |
intron_variant | MODIFIER | c.588+375delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | ||||||
chr1:46652205
|
CAA | C | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0171others(3): Show | 7 | HG02280.hp1 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+374_588+375del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | ||||||
chr1:46652272
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+309G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652272 | ||||||
chr1:46652375
|
CACTTATT others(48): Show |
C | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+151_588+205del others(55): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652375 | ||||||
chr1:46652395
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(144): Show | 263 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.588+186C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652395 | ||||||
chr1:46652424
|
C | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+157G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652424 | ||||||
chr1:46652496
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0017others(38): Show | 74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.588+85G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652496 | ||||||
chr1:46652517
|
G | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.588+64C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652517 | ||||||
chr1:46652570
|
C | T | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+11G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652570 | ||||||
chr1:46652900
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.541-272T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652900 | ||||||
chr1:46652929
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.541-301A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652929 | ||||||
chr1:46652972
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(238): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.541-344G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652972 | ||||||
chr1:46652990
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0244 | 8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-362G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652990 | ||||||
chr1:46653026
|
G | A | 4 | a0001c0001t0010g0195a0001c0001t0010g0196a0001c0001t0010g0243others(1): Show | 4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-398C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653026 | ||||||
chr1:46653246
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(157): Show | 280 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.540+571T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653246 | ||||||
chr1:46653352
|
A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+465T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653352 | ||||||
chr1:46653676
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.540+141G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653676 | ||||||
chr1:46654011
|
G | C | 1 | a0001c0001t0005g0238 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.490-144C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654011 | ||||||
chr1:46654091
|
G | A | 1 | a0001c0001t0005g0239 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.490-224C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654091 | ||||||
chr1:46654154
|
C | T | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-287G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654154 | ||||||
chr1:46654161
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.490-294A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654161 | ||||||
chr1:46654243
|
G | C | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-376C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654243 | ||||||
chr1:46654280
|
T | C | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-413A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654280 | ||||||
chr1:46654300
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.490-433T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654300 | ||||||
chr1:46654501
|
C | A | 1 | a0001c0001t0002g0053 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.490-634G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654501 | ||||||
chr1:46654527
|
A | ATTTAT | 45 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(42): Show | 88 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.490-665_490-661dup others(5): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654527 | ||||||
chr1:46654528
|
T | TTTA | 33 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0022others(30): Show | 56 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.490-664_490-662dup others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTA | 58 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0045others(55): Show | 109 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.490-667_490-662dup others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTAT others(2): Show |
12 | a0001c0001t0002g0012a0001c0001t0002g0047a0001c0001t0002g0048others(9): Show | 20 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-670_490-662dup others(9): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTAT others(5): Show |
2 | a0001c0001t0002g0049a0001c0001t0002g0211 | 3 | HG00408.hp1 HG02523.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.490-673_490-662dup others(12): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTTA others(3): Show |
1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-662_490-661ins others(10): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTTT others(1): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0171others(5): Show | 14 | HG00544.hp2 HG01243.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-662_490-661ins others(8): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTTT others(4): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0152others(3): Show | 6 | HG01884.hp2 HG02040.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-662_490-661ins others(11): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
T | TTTATTTT others(10): Show |
1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-662_490-661ins others(17): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654528
|
TTTA | T | 4 | a0001c0001t0003g0126a0002c0002t0004g0010a0002c0002t0004g0067others(1): Show | 8 | HG01358.hp1 HG01943.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-664_490-662del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | ||||||
chr1:46654531
|
A | ATT | 9 | a0001c0001t0001g0032a0001c0001t0001g0150a0001c0001t0001g0155others(6): Show | 14 | HG01891.hp2 HG02080.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-666_490-665dup others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654531 | ||||||
chr1:46654532
|
TTA | T | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-667_490-666del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654532 | ||||||
chr1:46654561
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(146): Show | 265 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.490-694C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654561 | ||||||
chr1:46654563
|
A | T | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-696T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654563 | ||||||
chr1:46654564
|
C | A | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-697G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654564 | ||||||
chr1:46654567
|
T | A | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-700A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654567 | ||||||
chr1:46654702
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.490-835G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654702 | ||||||
chr1:46654786
|
C | T | 2 | a0001c0001t0010g0195a0001c0001t0010g0196 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.490-919G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654786 | ||||||
chr1:46654997
|
G | A | 4 | a0001c0001t0010g0195a0001c0001t0010g0196a0001c0001t0010g0243others(1): Show | 4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-1130C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654997 | ||||||
chr1:46655001
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.490-1134T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655001 | ||||||
chr1:46655112
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-1245C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655112 | ||||||
chr1:46655271
|
C | T | 1 | a0001c0001t0019g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.490-1404G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655271 | ||||||
chr1:46655289
|
TA | T | 3 | a0001c0001t0002g0199a0001c0001t0002g0201a0001c0001t0029g0200 | 3 | HG00639.hp1 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.490-1423delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655289 | ||||||
chr1:46655294
|
T | C | 4 | a0001c0001t0010g0195a0001c0001t0010g0196a0001c0001t0010g0243others(1): Show | 4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-1427A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655294 | ||||||
chr1:46655694
|
T | C | 2 | a0001c0001t0002g0212a0001c0001t0002g0217 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-1827A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655694 | ||||||
chr1:46655747
|
T | C | 49 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(46): Show | 82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.490-1880A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655747 | ||||||
chr1:46655790
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.490-1923G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655790 | ||||||
chr1:46655830
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(64): Show | 117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.490-1963G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655830 | ||||||
chr1:46655869
|
A | T | 1 | a0001c0001t0004g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-2002T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655869 | ||||||
chr1:46655977
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-2110A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655977 | ||||||
chr1:46656060
|
G | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.489+2067C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656060 | ||||||
chr1:46656124
|
T | A | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2003A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656124 | ||||||
chr1:46656138
|
T | C | 1 | a0001c0001t0001g0032 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.489+1989A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656138 | ||||||
chr1:46656266
|
G | A | 1 | a0002c0002t0004g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.489+1861C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656266 | ||||||
chr1:46656269
|
G | A | 1 | a0001c0001t0023g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.489+1858C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656269 | ||||||
chr1:46656359
|
G | T | 1 | a0001c0001t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+1768C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656359 | ||||||
chr1:46656443
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | HG02486.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.489+1684G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656443 | ||||||
chr1:46656453
|
T | C | 1 | a0001c0001t0002g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.489+1674A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656453 | ||||||
chr1:46656460
|
T | C | 1 | a0001c0001t0006g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.489+1667A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656460 | ||||||
chr1:46656861
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0244 | 7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1266A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656861 | ||||||
chr1:46656870
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.489+1257G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656870 | ||||||
chr1:46656924
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+1203G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656924 | ||||||
chr1:46657049
|
G | C | 1 | a0001c0001t0006g0052 | 2 | HG02165.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.489+1078C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657049 | ||||||
chr1:46657153
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.489+974C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657153 | ||||||
chr1:46657184
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(52): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.489+943A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657184 | ||||||
chr1:46657261
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+866C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657261 | ||||||
chr1:46657300
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.489+827G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657300 | ||||||
chr1:46657344
|
C | A | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.489+783G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657344 | ||||||
chr1:46657410
|
C | T | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+717G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657410 | ||||||
chr1:46657606
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489+521C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657606 | ||||||
chr1:46657891
|
C | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+236G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657891 | ||||||
chr1:46657891
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.489+236G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657891 | ||||||
chr1:46657927
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+200G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657927 | ||||||
chr1:46658226
|
T | TA | 41 | a0001c0001t0002g0214a0001c0001t0005g0006a0001c0001t0005g0234others(38): Show | 59 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.427-38dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | ||||||
chr1:46658226
|
TA | T | 11 | a0001c0001t0002g0088a0001c0001t0002g0216a0001c0001t0002g0220others(8): Show | 15 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-38delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | ||||||
chr1:46658226
|
TAA | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(12): Show | 22 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.427-39_427-38delTT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | ||||||
chr1:46658226
|
TAAA | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(49): Show | 95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.427-40_427-38delTT others(1): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | ||||||
chr1:46658239
|
A | C | 1 | a0001c0001t0003g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.427-50T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658239 | ||||||
chr1:46658478
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.426+209C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658478 | ||||||
chr1:46658532
|
C | CA | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.426+154dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658532 | ||||||
chr1:46658642
|
C | T | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+45G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658642 | ||||||
chr1:46658807
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-70T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658807 | ||||||
chr1:46658882
|
T | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-145A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658882 | ||||||
chr1:46658930
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.376-193T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658930 | ||||||
chr1:46659018
|
C | T | 2 | a0001c0001t0010g0195a0001c0001t0010g0196 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.376-281G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659018 | ||||||
chr1:46659106
|
G | A | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-369C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659106 | ||||||
chr1:46659116
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(205): Show | 360 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.376-379T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659116 | ||||||
chr1:46659212
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(64): Show | 117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.376-475T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659212 | ||||||
chr1:46659327
|
C | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.376-590G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659327 | ||||||
chr1:46659365
|
TC | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-629delG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659365 | ||||||
chr1:46659419
|
C | T | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-682G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659419 | ||||||
chr1:46659513
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0244 | 8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-776G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659513 | ||||||
chr1:46659535
|
AT | A | 49 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(46): Show | 82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.376-799delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659535 | ||||||
chr1:46659611
|
G | A | 21 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0022others(18): Show | 43 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-874C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659611 | ||||||
chr1:46659900
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.376-1163A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659900 | ||||||
chr1:46659902
|
C | T | 2 | a0001c0001t0001g0032a0002c0002t0004g0057 | 3 | HG02559.hp2 HG03209.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.376-1165G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659902 | ||||||
chr1:46659916
|
C | T | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-1179G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659916 | ||||||
chr1:46659979
|
C | CT | 11 | a0001c0001t0003g0099a0001c0001t0005g0006a0001c0001t0005g0234others(8): Show | 18 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-1243dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659979 | ||||||
chr1:46659979
|
CT | C | 41 | a0001c0001t0001g0174a0001c0001t0002g0002a0001c0001t0002g0012others(38): Show | 73 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.376-1243delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659979 | ||||||
chr1:46660101
|
C | T | 3 | a0002c0002t0004g0025a0002c0002t0004g0060a0002c0002t0004g0061 | 4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.376-1364G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660101 | ||||||
chr1:46660225
|
C | A | 1 | a0001c0001t0006g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.376-1488G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660225 | ||||||
chr1:46660294
|
C | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(75): Show | 140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.376-1557G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660294 | ||||||
chr1:46660328
|
A | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0191a0001c0001t0002g0192others(2): Show | 6 | NA18951.hp2 NA18969.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1591T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660328 | ||||||
chr1:46660351
|
T | G | 1 | a0001c0001t0004g0029 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.376-1614A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660351 | ||||||
chr1:46660716
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0179a0001c0001t0001g0180 | 6 | NA18945.hp2 NA18950.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1979C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660716 | ||||||
chr1:46660719
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-1982T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660719 | ||||||
chr1:46660720
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(148): Show | 267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-1983A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660720 | ||||||
chr1:46660853
|
T | A | 1 | a0001c0001t0003g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.376-2116A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660853 | ||||||
chr1:46660860
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0175 | 3 | NA18979.hp1 NA18984.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.376-2123G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660860 | ||||||
chr1:46660953
|
CT | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2217delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660953 | ||||||
chr1:46660955
|
T | C | 49 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(46): Show | 82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.376-2218A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660955 | ||||||
chr1:46661076
|
G | GT | 12 | a0001c0001t0001g0154a0001c0001t0001g0244a0001c0001t0002g0191others(9): Show | 13 | HG01168.hp1 HG01243.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.376-2340dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661076 | ||||||
chr1:46661104
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2367T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661104 | ||||||
chr1:46661111
|
C | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(77): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.376-2374G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661111 | ||||||
chr1:46661120
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0244 | 8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2383A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661120 | ||||||
chr1:46661159
|
G | A | 1 | a0002c0002t0004g0025 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.376-2422C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661159 | ||||||
chr1:46661165
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-2428G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661165 | ||||||
chr1:46661268
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2531C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661268 | ||||||
chr1:46661370
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.376-2633G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661370 | ||||||
chr1:46661499
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0244 | 8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2762C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661499 | ||||||
chr1:46661505
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.376-2768C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661505 | ||||||
chr1:46661518
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2781A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661518 | ||||||
chr1:46661594
|
C | A | 21 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0022others(18): Show | 43 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-2857G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661594 | ||||||
chr1:46661680
|
T | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0141a0001c0001t0001g0143others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-2943A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661680 | ||||||
chr1:46661709
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(52): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.376-2972C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661709 | ||||||
chr1:46661776
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0040others(7): Show | 18 | HG00673.hp1 HG02132.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.376-3039C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661776 | ||||||
chr1:46661893
|
C | CT | 5 | a0001c0001t0003g0093a0001c0001t0003g0096a0001c0001t0003g0097others(2): Show | 5 | HG03130.hp1 NA18970.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-3157dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661893 | ||||||
chr1:46661893
|
C | CTT | 4 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0014g0144others(1): Show | 5 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-3158_376-3157d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661893 | ||||||
chr1:46661896
|
TC | T | 33 | a0001c0001t0001g0041a0001c0001t0001g0143a0001c0001t0001g0181others(30): Show | 56 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.376-3160delG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661896 | ||||||
chr1:46661897
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(173): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.376-3160G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661897 | ||||||
chr1:46661934
|
G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-3197C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661934 | ||||||
chr1:46662092
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+3164G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662092 | ||||||
chr1:46662116
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.375+3140T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662116 | ||||||
chr1:46662164
|
C | G | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.375+3092G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662164 | ||||||
chr1:46662312
|
CTA | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2942_375+2943d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662312 | ||||||
chr1:46662383
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.375+2873C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662383 | ||||||
chr1:46662396
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+2860A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662396 | ||||||
chr1:46662451
|
A | AT | 80 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(77): Show | 142 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.375+2804dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662451 | ||||||
chr1:46662706
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG01884.hp2 HG03225.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.375+2550G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662706 | ||||||
chr1:46662720
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0128 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.375+2536G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662720 | ||||||
chr1:46662923
|
C | A | 1 | a0001c0001t0002g0053 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.375+2333G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662923 | ||||||
chr1:46663002
|
G | A | 2 | a0001c0001t0003g0124a0001c0001t0003g0125 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.375+2254C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663002 | ||||||
chr1:46663009
|
A | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2247T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663009 | ||||||
chr1:46663012
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+2244G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663012 | ||||||
chr1:46663014
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.375+2242A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663014 | ||||||
chr1:46663043
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+2213A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663043 | ||||||
chr1:46663107
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.375+2149A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663107 | ||||||
chr1:46663148
|
T | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.375+2108A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663148 | ||||||
chr1:46663150
|
T | C | 1 | a0002c0002t0004g0084 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.375+2106A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663150 | ||||||
chr1:46663355
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(65): Show | 121 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.375+1901G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663355 | ||||||
chr1:46663602
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.375+1654A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663602 | ||||||
chr1:46663627
|
GT | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+1628delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663627 | ||||||
chr1:46663747
|
C | G | 1 | a0001c0001t0003g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.375+1509G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663747 | ||||||
chr1:46664078
|
T | G | 8 | a0001c0001t0005g0006a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.375+1178A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664078 | ||||||
chr1:46664187
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.375+1069A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664187 | ||||||
chr1:46664189
|
T | A | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.375+1067A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664189 | ||||||
chr1:46664336
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.375+920G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664336 | ||||||
chr1:46664407
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.375+849C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664407 | ||||||
chr1:46664435
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+821G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664435 | ||||||
chr1:46664460
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.375+796G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664460 | ||||||
chr1:46664645
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+611C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664645 | ||||||
chr1:46664776
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+480C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664776 | ||||||
chr1:46664861
|
T | C | 1 | a0001c0001t0023g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.375+395A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664861 | ||||||
chr1:46664865
|
T | G | 1 | a0001c0001t0003g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.375+391A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664865 | ||||||
chr1:46664922
|
C | T | 37 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0018others(34): Show | 69 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.375+334G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664922 | ||||||
chr1:46664956
|
C | T | 136 | a0001c0001t0001g0150a0001c0001t0002g0002a0001c0001t0002g0004others(133): Show | 234 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.375+300G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664956 | ||||||
chr1:46664972
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.375+284G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664972 | ||||||
chr1:46665042
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.375+214C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46665042 | ||||||
chr1:46665201
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(151): Show | 264 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.375+55T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46665201 | ||||||
chr1:46665435
|
T | G | 2 | a0001c0001t0002g0242a0001c0001t0021g0241 | 2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.267-71A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665435 | ||||||
chr1:46665534
|
A | G | 2 | a0001c0001t0016g0187a0001c0001t0016g0188 | 2 | HG00642.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.267-170T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665534 | ||||||
chr1:46665576
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-212C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665576 | ||||||
chr1:46665647
|
A | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-283T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665647 | ||||||
chr1:46665738
|
C | G | 1 | a0001c0001t0019g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.267-374G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665738 | ||||||
chr1:46665858
|
G | A | 1 | a0001c0001t0001g0016 | 4 | HG02486.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267-494C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665858 | ||||||
chr1:46665923
|
A | T | 2 | a0001c0001t0003g0091a0001c0001t0003g0092 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.267-559T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665923 | ||||||
chr1:46666062
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG00642.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.267-698G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666062 | ||||||
chr1:46666108
|
C | A | 5 | a0001c0001t0009g0034a0001c0001t0009g0146a0001c0001t0009g0147others(2): Show | 6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.267-744G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666108 | ||||||
chr1:46666237
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0244 | 8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.267-873C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666237 | ||||||
chr1:46666310
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-946C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666310 | ||||||
chr1:46666345
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(52): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.267-981G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666345 | ||||||
chr1:46666350
|
G | A | 8 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(5): Show | 11 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.267-986C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666350 | ||||||
chr1:46666548
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267-1184T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666548 | ||||||
chr1:46666571
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0008others(76): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.267-1207A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666571 | ||||||
chr1:46666642
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.267-1278A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666642 | ||||||
chr1:46666774
|
G | A | 2 | a0002c0002t0004g0086a0002c0002t0004g0087 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.266+1283C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666774 | ||||||
chr1:46666848
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+1209G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666848 | ||||||
chr1:46667050
|
T | C | 1 | a0001c0001t0010g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266+1007A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667050 | ||||||
chr1:46667232
|
TGGA | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0244 | 7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+822_266+824del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667232 | ||||||
chr1:46667236
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0244 | 7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+821T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667236 | ||||||
chr1:46667237
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0244 | 7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+820C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667237 | ||||||
chr1:46667342
|
T | C | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.266+715A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667342 | ||||||
chr1:46667388
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.266+669A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667388 | ||||||
chr1:46667617
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266+440G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667617 | ||||||
chr1:46667743
|
T | C | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.266+314A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667743 | ||||||
chr1:46667803
|
G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+254C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667803 | ||||||
chr1:46667910
|
G | A | 2 | a0001c0001t0015g0247a0001c0001t0015g0248 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.266+147C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667910 |