geneid | 2309 |
---|---|
ensemblid | ENSG00000118689.15 |
hgncid | 3821 |
symbol | FOXO3 |
name | forkhead box O3 |
refseq_nuc | NM_001455.4 |
refseq_prot | NP_001446.1 |
ensembl_nuc | ENST00000406360.2 |
ensembl_prot | ENSP00000385824.1 |
mane_status | MANE Select |
chr | chr6 |
start | 108560917 |
end | 108684774 |
strand | + |
ver | v1.2 |
region | chr6:108560917-108684774 |
region5000 | chr6:108555917-108689774 |
regionname0 | FOXO3_chr6_108560917_108684774 |
regionname5000 | FOXO3_chr6_108555917_108689774 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 673 | 273 | 87 | 40 | 95 | 16 | 33 | 68 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0002 | 0/0 | 673 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0003 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0004 | 0/0 | 673 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2022 | 214 | 70 | 25 | 81 | 13 | 24 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0002 | 0/1 | 2022 | 54 | 17 | 15 | 11 | 3 | 7 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0003 | 0/0 | 2022 | 3 | 0 | 0 | 2 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0004 | 0/0 | 2022 | 3 | 0 | 2 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0005 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0006 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0007 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
c0008 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5277 | 83 | 7 | 19 | 36 | 9 | 12 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0002 | 0/1 | 5275 | 53 | 24 | 12 | 8 | 2 | 6 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0003 | 0/0 | 5276 | 49 | 9 | 1 | 30 | 3 | 6 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0004 | 0/0 | 5275 | 8 | 7 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0005 | 0/0 | 5272 | 7 | 6 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0006 | 0/0 | 5276 | 7 | 3 | 0 | 3 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0007 | 0/0 | 5275 | 7 | 6 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0008 | 0/0 | 5278 | 6 | 1 | 1 | 4 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0009 | 0/0 | 5272 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0010 | 0/0 | 5275 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0011 | 0/0 | 5275 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0012 | 0/0 | 5276 | 3 | 0 | 0 | 3 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0013 | 0/0 | 5275 | 3 | 3 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0014 | 0/0 | 5277 | 2 | 1 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0015 | 0/0 | 5276 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0016 | 0/0 | 5276 | 2 | 0 | 0 | 1 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0017 | 0/0 | 5276 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0018 | 0/0 | 5277 | 2 | 0 | 1 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0019 | 0/0 | 5276 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0020 | 0/0 | 5275 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0021 | 0/0 | 5276 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0022 | 0/0 | 5272 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0023 | 0/0 | 5277 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0024 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0025 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0026 | 0/0 | 5277 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0027 | 0/0 | 5276 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0028 | 0/0 | 5276 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0029 | 0/0 | 5277 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0030 | 0/0 | 5277 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0031 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0032 | 0/0 | 5277 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0033 | 0/0 | 5275 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0034 | 0/0 | 5276 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0035 | 0/0 | 5276 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0036 | 0/0 | 5277 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0037 | 1/0 | 5275 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0038 | 0/0 | 5275 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0039 | 0/0 | 5275 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0040 | 0/0 | 5275 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0041 | 0/0 | 5276 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0042 | 0/0 | 5277 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0043 | 0/0 | 5275 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0044 | 0/0 | 5276 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
t0045 | 0/0 | 5277 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2022 | 214 | 70 | 25 | 81 | 13 | 24 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002 | 0/1 | 2022 | 54 | 17 | 15 | 11 | 3 | 7 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0003 | 0/0 | 2022 | 3 | 0 | 0 | 2 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0006 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0007 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0002c0004 | 0/0 | 2022 | 3 | 0 | 2 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0003c0005 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0004c0008 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7298 | 76 | 7 | 16 | 34 | 8 | 11 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0002 | 0/0 | 7296 | 11 | 10 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0003 | 0/0 | 7297 | 47 | 9 | 1 | 28 | 3 | 6 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0004 | 0/0 | 7296 | 8 | 7 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0005 | 0/0 | 7293 | 7 | 6 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0006 | 0/0 | 7297 | 6 | 3 | 0 | 3 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0007 | 0/0 | 7296 | 6 | 5 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0008 | 0/0 | 7299 | 6 | 1 | 1 | 4 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0009 | 0/0 | 7293 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0010 | 0/0 | 7296 | 3 | 3 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0011 | 0/0 | 7296 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0012 | 0/0 | 7297 | 3 | 0 | 0 | 3 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0013 | 0/0 | 7296 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0014 | 0/0 | 7298 | 2 | 1 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0015 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0017 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0018 | 0/0 | 7298 | 2 | 0 | 1 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0020 | 0/0 | 7296 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0021 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0022 | 0/0 | 7293 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0023 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0024 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0025 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0026 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0027 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0028 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0029 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0030 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0031 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0032 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0033 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0034 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0037 | 1/0 | 7296 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0040 | 0/0 | 7296 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0041 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0042 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0043 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0044 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0001t0045 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0001 | 0/0 | 7298 | 2 | 0 | 1 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0002 | 0/1 | 7296 | 42 | 14 | 12 | 8 | 2 | 5 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0003 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0010 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0013 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0019 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0021 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0035 | 0/0 | 7297 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0036 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0038 | 0/0 | 7296 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0002t0039 | 0/0 | 7296 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0003t0003 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0003t0016 | 0/0 | 7297 | 2 | 0 | 0 | 1 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0006t0001 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0001c0007t0006 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0002c0004t0001 | 0/0 | 7298 | 3 | 0 | 2 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0003c0005t0007 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
a0004c0008t0001 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | copy fasta | chr6 | 108555917 | 108689774 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0014g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0015g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0015g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0017g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0018g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0018g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0022g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0023g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0024g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0025g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0026g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0027g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0028g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0029g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0030g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0031g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0032g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0033g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0034g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0037g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0040g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0041g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0042g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0043g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0044g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0001t0045g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0019g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0035g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0036g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0038g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0002t0039g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0003t0016g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0003t0016g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0001c0007t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0002c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0002c0004t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0002c0004t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0003c0005t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
a0004c0008t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0018 | g0121 | EUR | GBR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0187 | EUR | GBR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0213 | EUR | FIN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00323 | hp2 | a0001 | c0001 | t0027 | g0261 | EUR | FIN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00621 | hp2 | a0001 | c0001 | t0025 | g0218 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00673 | hp1 | a0001 | c0001 | t0015 | g0217 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00673 | hp2 | a0001 | c0001 | t0017 | g0107 | EAS | CHS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG00735 | hp2 | a0002 | c0004 | t0001 | g0013 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01074 | hp2 | a0002 | c0004 | t0001 | g0014 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01106 | hp1 | a0001 | c0001 | t0030 | g0079 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01106 | hp2 | a0001 | c0001 | t0040 | g0032 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01256 | hp2 | a0001 | c0002 | t0038 | g0181 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01257 | hp2 | a0001 | c0001 | t0023 | g0119 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0095 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0188 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0205 | EUR | IBS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0206 | EUR | IBS | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01934 | hp1 | a0001 | c0002 | t0035 | g0164 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01934 | hp2 | a0001 | c0001 | t0018 | g0120 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0176 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0162 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02004 | hp1 | a0001 | c0001 | t0042 | g0043 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02071 | hp1 | a0004 | c0008 | t0001 | g0256 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02132 | hp2 | a0001 | c0001 | t0031 | g0068 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | CDX | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0245 | EAS | CDX | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0047 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0129 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02622 | hp1 | a0001 | c0001 | t0044 | g0260 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0210 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02630 | hp1 | a0001 | c0001 | t0033 | g0006 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0123 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02683 | hp1 | a0001 | c0001 | t0026 | g0249 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02738 | hp1 | a0001 | c0002 | t0036 | g0172 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02818 | hp2 | a0001 | c0002 | t0013 | g0234 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02976 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03017 | hp1 | a0001 | c0001 | t0014 | g0267 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03041 | hp2 | a0001 | c0001 | t0020 | g0018 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03098 | hp2 | a0001 | c0001 | t0013 | g0021 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03139 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | ESN | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03225 | hp2 | a0001 | c0002 | t0021 | g0185 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03239 | hp1 | a0001 | c0002 | t0039 | g0182 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03239 | hp2 | a0002 | c0004 | t0001 | g0012 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0189 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03486 | hp1 | a0001 | c0002 | t0010 | g0192 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03490 | hp2 | a0001 | c0001 | t0028 | g0277 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03540 | hp1 | a0001 | c0001 | t0034 | g0246 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0146 | AFR | GWD | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03579 | hp1 | a0001 | c0001 | t0043 | g0046 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03654 | hp1 | a0001 | c0001 | t0041 | g0051 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0253 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0177 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03834 | hp1 | a0001 | c0001 | t0045 | g0067 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0175 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04199 | hp1 | a0001 | c0007 | t0006 | g0251 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04199 | hp2 | a0001 | c0001 | t0029 | g0044 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG04204 | hp2 | a0001 | c0003 | t0016 | g0240 | SAS | STU | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CHB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | YRI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | YRI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18940 | hp1 | a0001 | c0002 | t0019 | g0179 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18954 | hp1 | a0001 | c0001 | t0032 | g0143 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18967 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0173 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18969 | hp2 | a0001 | c0001 | t0024 | g0229 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18970 | hp2 | a0001 | c0003 | t0003 | g0225 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18975 | hp1 | a0001 | c0001 | t0017 | g0071 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18981 | hp1 | a0001 | c0001 | t0008 | g0100 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18999 | hp2 | a0001 | c0001 | t0015 | g0201 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19011 | hp2 | a0001 | c0003 | t0016 | g0154 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0174 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19043 | hp1 | a0003 | c0005 | t0007 | g0031 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19057 | hp1 | a0001 | c0001 | t0012 | g0199 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19066 | hp2 | a0001 | c0006 | t0001 | g0080 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19083 | hp2 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19088 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | YRI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ASW | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0254 | EUR | TSI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0178 | EUR | TSI | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | GIH | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0159 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | ACB | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0128 | AFR | MSL | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG06807 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | USA | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA18955 | hp2 | a0001 | c0002 | t0019 | g0157 | EAS | JPT | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20300 | hp1 | a0001 | c0001 | t0021 | g0015 | AFR | USA | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | USA | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
NA21309 | hp2 | a0001 | c0001 | t0022 | g0136 | AFR | LWK | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0212 | REF | REF | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0037 | g0126 | REF | REF | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108561627
|
C | T | 1 | a0002 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.419C>T | p.Ala140Val | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/3 | 711/7296 | 419/2022 | 140/673 | chr6 | 108561627 | ||
chr6:108561798
|
A | G | 1 | a0004 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.590A>G | p.Lys197Arg | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/3 | 882/7296 | 590/2022 | 197/673 | chr6 | 108561798 | ||
chr6:108664358
|
G | A | 1 | a0003 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1525G>A | p.Val509Met | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/3 | 1817/7296 | 1525/2022 | 509/673 | chr6 | 108664358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108561367
|
C | T | 1 | a0001c0002 | 54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): Show |
synonymous_variant | LOW | c.159C>T | p.Ala53Ala | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/3 | 451/7296 | 159/2022 | 53/673 | chr6 | 108561367 | ||
chr6:108663673
|
A | T | 1 | a0001c0007 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.840A>T | p.Ser280Ser | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/3 | 1132/7296 | 840/2022 | 280/673 | chr6 | 108663673 | ||
chr6:108663847
|
C | T | 1 | a0001c0006 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1014C>T | p.Asp338Asp | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/3 | 1306/7296 | 1014/2022 | 338/673 | chr6 | 108663847 | ||
chr6:108664018
|
G | A | 1 | a0001c0003 | 3 | HG04204.hp2 NA18970.hp2 NA19011.hp2 |
synonymous_variant | LOW | c.1185G>A | p.Thr395Thr | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/3 | 1477/7296 | 1185/2022 | 395/673 | chr6 | 108664018 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108560922
|
C | T | 1 | a0001c0001t0045 | 1 | HG03834.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-287C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/3 | chr6 | 108560922 | ||||||
chr6:108680001
|
A | T | 1 | a0001c0001t0044 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15146 | chr6 | 108680001 | |||||
chr6:108680168
|
GTGT | G | 3 | a0001c0001t0005a0001c0001t0009a0001c0001t0022 | 12 | HG02135.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*381_*383delGTT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15318 | INFO_REALIGN_3_PRIME | chr6 | 108680168 | ||||
chr6:108680251
|
A | C | 1 | a0001c0001t0043 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15396 | chr6 | 108680251 | |||||
chr6:108680415
|
T | C | 1 | a0001c0001t0012 | 3 | NA18968.hp1 NA19010.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15560 | chr6 | 108680415 | |||||
chr6:108680575
|
A | G | 1 | a0001c0001t0009 | 4 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*783A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15720 | chr6 | 108680575 | |||||
chr6:108680575
|
A | T | 1 | a0001c0001t0042 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15720 | chr6 | 108680575 | |||||
chr6:108680751
|
G | GA | 27 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(24): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*973dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15911 | INFO_REALIGN_3_PRIME | chr6 | 108680751 | ||||
chr6:108680751
|
G | GAA | 2 | a0001c0001t0008a0001c0001t0014 | 8 | HG00438.hp1 HG01358.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*972_*973dupAA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15911 | INFO_REALIGN_3_PRIME | chr6 | 108680751 | ||||
chr6:108680766
|
C | A | 1 | a0001c0001t0023 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*974C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15911 | chr6 | 108680766 | |||||
chr6:108680839
|
C | T | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(14): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1047C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 15984 | chr6 | 108680839 | |||||
chr6:108680950
|
G | T | 2 | a0001c0001t0007a0003c0005t0007 | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1158G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16095 | chr6 | 108680950 | |||||
chr6:108681755
|
G | A | 1 | a0001c0001t0029 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1963G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16900 | chr6 | 108681755 | |||||
chr6:108681793
|
C | T | 1 | a0001c0001t0040 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2001C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16938 | chr6 | 108681793 | |||||
chr6:108681832
|
A | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16977 | chr6 | 108681832 | |||||
chr6:108681833
|
A | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2041A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16978 | chr6 | 108681833 | |||||
chr6:108681835
|
A | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16980 | chr6 | 108681835 | |||||
chr6:108681839
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16984 | chr6 | 108681839 | |||||
chr6:108681840
|
T | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2048T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16985 | chr6 | 108681840 | |||||
chr6:108681843
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16988 | chr6 | 108681843 | |||||
chr6:108681844
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16989 | chr6 | 108681844 | |||||
chr6:108681845
|
A | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16990 | chr6 | 108681845 | |||||
chr6:108681846
|
C | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16991 | chr6 | 108681846 | |||||
chr6:108681849
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16994 | chr6 | 108681849 | |||||
chr6:108681850
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2058C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 16995 | chr6 | 108681850 | |||||
chr6:108681883
|
C | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17028 | chr6 | 108681883 | |||||
chr6:108681886
|
T | C | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17031 | chr6 | 108681886 | |||||
chr6:108681887
|
C | A | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17032 | chr6 | 108681887 | |||||
chr6:108681888
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17033 | chr6 | 108681888 | |||||
chr6:108681889
|
A | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17034 | chr6 | 108681889 | |||||
chr6:108681892
|
A | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2100A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17037 | chr6 | 108681892 | |||||
chr6:108681899
|
A | C | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17044 | chr6 | 108681899 | |||||
chr6:108681901
|
G | A | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17046 | chr6 | 108681901 | |||||
chr6:108681904
|
G | C | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2112G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17049 | chr6 | 108681904 | |||||
chr6:108681905
|
G | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17050 | chr6 | 108681905 | |||||
chr6:108681908
|
T | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2116T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17053 | chr6 | 108681908 | |||||
chr6:108681909
|
G | A | 2 | a0001c0001t0030a0001c0002t0039 | 2 | HG01106.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2117G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17054 | chr6 | 108681909 | |||||
chr6:108681910
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17055 | chr6 | 108681910 | |||||
chr6:108681911
|
C | T | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17056 | chr6 | 108681911 | |||||
chr6:108681912
|
T | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2120T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17057 | chr6 | 108681912 | |||||
chr6:108681920
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2128C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17065 | chr6 | 108681920 | |||||
chr6:108681923
|
C | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2131C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17068 | chr6 | 108681923 | |||||
chr6:108681926
|
A | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17071 | chr6 | 108681926 | |||||
chr6:108681932
|
T | C | 2 | a0001c0001t0004a0001c0001t0033 | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2140T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17077 | chr6 | 108681932 | |||||
chr6:108681939
|
C | A | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2147C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17084 | chr6 | 108681939 | |||||
chr6:108681942
|
T | G | 1 | a0001c0002t0039 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2150T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17087 | chr6 | 108681942 | |||||
chr6:108681945
|
G | A | 1 | a0001c0001t0020 | 2 | HG02976.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2153G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17090 | chr6 | 108681945 | |||||
chr6:108682085
|
T | C | 1 | a0001c0001t0034 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2293T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17230 | chr6 | 108682085 | |||||
chr6:108682118
|
T | C | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(14): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2326T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17263 | chr6 | 108682118 | |||||
chr6:108682120
|
A | G | 1 | a0001c0001t0044 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17265 | chr6 | 108682120 | |||||
chr6:108682646
|
C | T | 1 | a0001c0001t0011 | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2854C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17791 | chr6 | 108682646 | |||||
chr6:108682677
|
G | A | 1 | a0001c0001t0015 | 2 | HG00673.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2885G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17822 | chr6 | 108682677 | |||||
chr6:108682786
|
C | A | 18 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(15): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2994C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17931 | chr6 | 108682786 | |||||
chr6:108682786
|
C | T | 1 | a0001c0001t0028 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2994C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17931 | chr6 | 108682786 | |||||
chr6:108682834
|
G | A | 2 | a0001c0001t0013a0001c0002t0013 | 3 | HG02818.hp2 HG03098.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 17979 | chr6 | 108682834 | |||||
chr6:108682855
|
G | C | 1 | a0001c0001t0024 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3063G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18000 | chr6 | 108682855 | |||||
chr6:108682865
|
T | C | 1 | a0001c0001t0031 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18010 | chr6 | 108682865 | |||||
chr6:108683176
|
C | T | 1 | a0001c0001t0018 | 2 | HG00099.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3384C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18321 | chr6 | 108683176 | |||||
chr6:108683300
|
T | A | 1 | a0001c0001t0025 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3508T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18445 | chr6 | 108683300 | |||||
chr6:108683686
|
C | CA | 18 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(15): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*3910dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18848 | INFO_REALIGN_3_PRIME | chr6 | 108683686 | ||||
chr6:108683810
|
T | TA | 5 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(2): Show | 10 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4029dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18967 | INFO_REALIGN_3_PRIME | chr6 | 108683810 | ||||
chr6:108683821
|
A | T | 1 | a0001c0001t0027 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4029A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18966 | chr6 | 108683821 | |||||
chr6:108683822
|
T | A | 1 | a0001c0001t0040 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4030T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 18967 | chr6 | 108683822 | |||||
chr6:108683880
|
C | G | 1 | a0001c0001t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4088C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19025 | chr6 | 108683880 | |||||
chr6:108683958
|
C | T | 2 | a0001c0001t0010a0001c0002t0010 | 4 | HG02965.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4166C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19103 | chr6 | 108683958 | |||||
chr6:108683959
|
G | A | 1 | a0001c0001t0032 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4167G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19104 | chr6 | 108683959 | |||||
chr6:108683971
|
A | G | 1 | a0001c0002t0038 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4179A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19116 | chr6 | 108683971 | |||||
chr6:108684283
|
A | T | 1 | a0001c0003t0016 | 2 | HG04204.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4491A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19428 | chr6 | 108684283 | |||||
chr6:108684385
|
A | G | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(36): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*4593A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19530 | chr6 | 108684385 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108561840
|
A | G | 1 | a0001c0002t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.621+11A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108561840 | ||||||
chr6:108561930
|
A | T | 19 | a0001c0001t0001g0259a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+101A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108561930 | ||||||
chr6:108562240
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+411C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562240 | ||||||
chr6:108562483
|
C | A | 29 | a0001c0001t0001g0259a0001c0001t0002g0258a0001c0001t0003g0262others(26): Show | 29 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.621+654C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562483 | ||||||
chr6:108562496
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.621+667A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562496 | ||||||
chr6:108562595
|
G | A | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.621+766G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562595 | ||||||
chr6:108562643
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+814G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562643 | ||||||
chr6:108562683
|
T | G | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+854T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562683 | ||||||
chr6:108562701
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+872G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562701 | ||||||
chr6:108562876
|
C | T | 1 | a0004c0008t0001g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.621+1047C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562876 | ||||||
chr6:108562927
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.621+1098C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562927 | ||||||
chr6:108562943
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.621+1114G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562943 | ||||||
chr6:108562954
|
T | C | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+1125T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562954 | ||||||
chr6:108562956
|
C | T | 6 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(3): Show | 6 | HG02155.hp1 HG02698.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+1127C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108562956 | ||||||
chr6:108562995
|
AT | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+1175delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108562995 | |||||
chr6:108563206
|
T | G | 29 | a0001c0001t0001g0259a0001c0001t0002g0258a0001c0001t0003g0262others(26): Show | 29 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.621+1377T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563206 | ||||||
chr6:108563262
|
A | T | 1 | a0001c0002t0002g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.621+1433A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563262 | ||||||
chr6:108563364
|
C | T | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+1535C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563364 | ||||||
chr6:108563366
|
A | G | 1 | a0001c0002t0002g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.621+1537A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563366 | ||||||
chr6:108563524
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.621+1695G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563524 | ||||||
chr6:108563532
|
C | T | 28 | a0001c0001t0002g0258a0001c0001t0003g0262a0001c0001t0003g0263others(25): Show | 28 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.621+1703C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563532 | ||||||
chr6:108563678
|
C | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+1849C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563678 | ||||||
chr6:108563688
|
C | T | 18 | a0001c0001t0003g0262a0001c0001t0003g0263a0001c0001t0003g0264others(15): Show | 18 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.621+1859C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563688 | ||||||
chr6:108563839
|
T | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+2010T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563839 | ||||||
chr6:108563843
|
C | T | 1 | a0001c0001t0003g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.621+2014C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563843 | ||||||
chr6:108563938
|
A | T | 1 | a0001c0001t0002g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.621+2109A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108563938 | ||||||
chr6:108563957
|
G | GT | 6 | a0001c0001t0001g0239a0001c0001t0002g0242a0001c0001t0002g0243others(3): Show | 6 | HG01433.hp2 HG01981.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2140dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108563957 | |||||
chr6:108564238
|
C | T | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.621+2409C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564238 | ||||||
chr6:108564295
|
T | G | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+2466T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564295 | ||||||
chr6:108564420
|
C | T | 97 | a0001c0001t0002g0152a0001c0001t0002g0208a0001c0001t0002g0242others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.621+2591C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564420 | ||||||
chr6:108564439
|
C | G | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+2610C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564439 | ||||||
chr6:108564549
|
C | T | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+2720C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564549 | ||||||
chr6:108564621
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.621+2792T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564621 | ||||||
chr6:108564656
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+2827C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564656 | ||||||
chr6:108564726
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0032g0143 | 3 | HG02155.hp2 NA18954.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.621+2897A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564726 | ||||||
chr6:108564783
|
G | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+2954G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564783 | ||||||
chr6:108564790
|
GT | G | 243 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.621+2972delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108564790 | |||||
chr6:108564907
|
A | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+3078A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564907 | ||||||
chr6:108564942
|
G | A | 2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.621+3113G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108564942 | ||||||
chr6:108565026
|
A | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+3197A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565026 | ||||||
chr6:108565041
|
A | G | 2 | a0001c0002t0002g0236a0001c0002t0002g0255 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.621+3212A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565041 | ||||||
chr6:108565212
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.621+3383T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565212 | ||||||
chr6:108565279
|
A | T | 1 | a0001c0001t0005g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+3450A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565279 | ||||||
chr6:108565387
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.621+3558T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565387 | ||||||
chr6:108565466
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.621+3637G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565466 | ||||||
chr6:108565475
|
G | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+3646G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565475 | ||||||
chr6:108565556
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+3727G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565556 | ||||||
chr6:108565615
|
G | T | 1 | a0001c0002t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.621+3786G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565615 | ||||||
chr6:108565616
|
T | C | 1 | a0001c0002t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.621+3787T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565616 | ||||||
chr6:108565638
|
TCTG | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+3826_621+3828d others(5): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108565638 | |||||
chr6:108565655
|
T | C | 1 | a0001c0002t0002g0149 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.621+3826T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565655 | ||||||
chr6:108565769
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02293.hp1 HG02300.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+3940G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565769 | ||||||
chr6:108565820
|
C | G | 4 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0235others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+3991C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565820 | ||||||
chr6:108565914
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+4085C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565914 | ||||||
chr6:108565933
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.621+4104T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108565933 | ||||||
chr6:108566051
|
C | A | 1 | a0001c0001t0004g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.621+4222C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566051 | ||||||
chr6:108566101
|
G | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+4272G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566101 | ||||||
chr6:108566163
|
C | T | 4 | a0001c0001t0008g0122a0001c0001t0018g0120a0001c0001t0018g0121others(1): Show | 4 | HG00099.hp1 HG01257.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+4334C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566163 | ||||||
chr6:108566172
|
C | T | 2 | a0001c0002t0002g0230a0001c0002t0002g0231 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.621+4343C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566172 | ||||||
chr6:108566355
|
C | T | 32 | a0001c0001t0002g0258a0001c0001t0003g0262a0001c0001t0003g0263others(29): Show | 32 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.621+4526C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566355 | ||||||
chr6:108566516
|
T | G | 1 | a0001c0001t0003g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.621+4687T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566516 | ||||||
chr6:108566847
|
A | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+5018A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108566847 | ||||||
chr6:108567138
|
CTT | C | 4 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(1): Show | 4 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+5316_621+5317d others(4): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108567138 | |||||
chr6:108567148
|
C | T | 4 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(1): Show | 4 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+5319C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567148 | ||||||
chr6:108567167
|
T | C | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.621+5338T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567167 | ||||||
chr6:108567178
|
A | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+5349A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567178 | ||||||
chr6:108567224
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.621+5395A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567224 | ||||||
chr6:108567237
|
A | G | 271 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.621+5408A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567237 | ||||||
chr6:108567327
|
G | T | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+5498G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567327 | ||||||
chr6:108567390
|
C | G | 109 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.621+5561C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567390 | ||||||
chr6:108567580
|
C | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+5751C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567580 | ||||||
chr6:108567618
|
C | T | 1 | a0001c0001t0024g0229 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.621+5789C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567618 | ||||||
chr6:108567665
|
T | G | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+5836T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567665 | ||||||
chr6:108567755
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+5926A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567755 | ||||||
chr6:108567799
|
C | A | 12 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(9): Show | 12 | HG01884.hp1 HG02922.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.621+5970C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567799 | ||||||
chr6:108567817
|
T | C | 35 | a0001c0001t0002g0258a0001c0001t0003g0262a0001c0001t0003g0263others(32): Show | 35 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.621+5988T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567817 | ||||||
chr6:108567861
|
A | G | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+6032A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108567861 | ||||||
chr6:108568029
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.621+6200C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568029 | ||||||
chr6:108568048
|
C | CA | 14 | a0001c0001t0001g0259a0001c0001t0004g0001a0001c0001t0004g0002others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.621+6233dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108568048 | |||||
chr6:108568178
|
C | G | 1 | a0001c0002t0002g0228 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.621+6349C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568178 | ||||||
chr6:108568215
|
CT | C | 36 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0151others(33): Show | 36 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.621+6402delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108568215 | |||||
chr6:108568217
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0002g0035a0001c0001t0010g0036 | 3 | HG02896.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.621+6388T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568217 | ||||||
chr6:108568294
|
G | A | 7 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+6465G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568294 | ||||||
chr6:108568428
|
T | C | 36 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0262others(33): Show | 36 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.621+6599T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568428 | ||||||
chr6:108568619
|
T | G | 37 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(34): Show | 37 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.621+6790T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568619 | ||||||
chr6:108568683
|
C | T | 1 | a0001c0001t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.621+6854C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568683 | ||||||
chr6:108568866
|
A | G | 29 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0262others(26): Show | 29 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.621+7037A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568866 | ||||||
chr6:108568929
|
GC | G | 19 | a0001c0001t0003g0037a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+7101delC | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568929 | ||||||
chr6:108568975
|
C | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.621+7146C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108568975 | ||||||
chr6:108569090
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.621+7261G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108569090 | ||||||
chr6:108569211
|
A | G | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+7382A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108569211 | ||||||
chr6:108569423
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG01943.hp2 NA18956.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.621+7594G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108569423 | ||||||
chr6:108569935
|
A | G | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+8106A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108569935 | ||||||
chr6:108569987
|
G | GT | 12 | a0001c0001t0005g0127a0001c0001t0005g0137a0001c0001t0005g0138others(9): Show | 12 | HG01192.hp2 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.621+8188dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTT | 21 | a0001c0001t0011g0145a0001c0002t0002g0149a0001c0002t0002g0158others(18): Show | 21 | HG01074.hp1 HG01243.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.621+8187_621+8188d others(4): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTT | 24 | a0001c0001t0010g0174a0001c0001t0011g0146a0001c0001t0012g0173others(21): Show | 24 | HG00140.hp2 HG01123.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.621+8186_621+8188d others(5): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTT | 12 | a0001c0001t0002g0242a0001c0001t0010g0189a0001c0001t0011g0147others(9): Show | 12 | HG01358.hp2 HG01884.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.621+8185_621+8188d others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTT | 23 | a0001c0001t0002g0208a0001c0001t0003g0150a0001c0001t0003g0151others(20): Show | 23 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.621+8184_621+8188d others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTTT | 13 | a0001c0001t0002g0243a0001c0001t0003g0214a0001c0001t0003g0215others(10): Show | 13 | HG00621.hp2 HG00673.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.621+8183_621+8188d others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTTTT | 5 | a0001c0001t0003g0224a0001c0001t0003g0226a0001c0001t0003g0227others(2): Show | 5 | HG02135.hp1 HG02717.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+8182_621+8188d others(9): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTTTT others(4): Show |
1 | a0002c0004t0001g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.621+8178_621+8188d others(13): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTTTT others(5): Show |
1 | a0002c0004t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.621+8177_621+8188d others(14): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
G | GTTTTTTT others(16): Show |
1 | a0002c0004t0001g0014 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621+8166_621+8188d others(25): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GT | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+8188delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTT | G | 6 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0004g0003others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+8185_621+8188d others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTT | G | 11 | a0001c0001t0003g0262a0001c0001t0003g0263a0001c0001t0003g0264others(8): Show | 11 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.621+8184_621+8188d others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTTT | G | 10 | a0001c0001t0003g0037a0001c0001t0003g0272a0001c0001t0003g0273others(7): Show | 10 | HG02155.hp1 HG02622.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+8183_621+8188d others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTTTT others(2): Show |
G | 12 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0040others(9): Show | 12 | HG00438.hp1 HG02145.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+8180_621+8188d others(11): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTTTT others(3): Show |
G | 94 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.621+8179_621+8188d others(12): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTTTT others(4): Show |
G | 4 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02004.hp1 NA18956.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+8178_621+8188d others(13): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108569987
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+8176_621+8188d others(15): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108569987 | |||||
chr6:108570038
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+8209C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570038 | ||||||
chr6:108570148
|
C | T | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+8319C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570148 | ||||||
chr6:108570175
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+8346A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570175 | ||||||
chr6:108570361
|
T | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+8532T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570361 | ||||||
chr6:108570517
|
T | C | 1 | a0001c0002t0002g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.621+8688T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570517 | ||||||
chr6:108570591
|
G | A | 1 | a0001c0001t0029g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.621+8762G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570591 | ||||||
chr6:108570836
|
A | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+9007A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570836 | ||||||
chr6:108570890
|
G | A | 1 | a0001c0001t0009g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.621+9061G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108570890 | ||||||
chr6:108571032
|
A | G | 19 | a0001c0001t0003g0037a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+9203A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571032 | ||||||
chr6:108571080
|
A | C | 1 | a0001c0001t0011g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.621+9251A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571080 | ||||||
chr6:108571149
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.621+9320C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571149 | ||||||
chr6:108571207
|
G | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+9378G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571207 | ||||||
chr6:108571459
|
C | G | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+9630C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571459 | ||||||
chr6:108571498
|
T | C | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+9669T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571498 | ||||||
chr6:108571500
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.621+9671G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571500 | ||||||
chr6:108571577
|
G | A | 1 | a0001c0001t0006g0245 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.621+9748G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571577 | ||||||
chr6:108571645
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.621+9816G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571645 | ||||||
chr6:108571647
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.621+9818C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571647 | ||||||
chr6:108571696
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.621+9867A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108571696 | ||||||
chr6:108572462
|
C | A | 1 | a0001c0002t0036g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.621+10633C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572462 | ||||||
chr6:108572509
|
C | G | 20 | a0001c0001t0001g0117a0001c0001t0003g0037a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+10680C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572509 | ||||||
chr6:108572519
|
C | T | 2 | a0001c0001t0011g0145a0001c0001t0011g0146 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.621+10690C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572519 | ||||||
chr6:108572573
|
A | G | 7 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+10744A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572573 | ||||||
chr6:108572671
|
G | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+10842G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572671 | ||||||
chr6:108572724
|
CTAA | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+10900_621+1090 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108572724 | |||||
chr6:108572979
|
T | C | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+11150T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108572979 | ||||||
chr6:108573013
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.621+11184G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573013 | ||||||
chr6:108573204
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.621+11375G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573204 | ||||||
chr6:108573235
|
C | T | 98 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.621+11406C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573235 | ||||||
chr6:108573280
|
CTG | C | 19 | a0001c0001t0003g0037a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+11453_621+1145 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108573280 | |||||
chr6:108573299
|
A | ATAAG | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+11486_621+1148 others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108573299 | |||||
chr6:108573509
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.621+11680C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573509 | ||||||
chr6:108573566
|
G | A | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+11737G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573566 | ||||||
chr6:108573753
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+11924C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573753 | ||||||
chr6:108573868
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+12039T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573868 | ||||||
chr6:108573879
|
C | T | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+12050C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108573879 | ||||||
chr6:108573953
|
AC | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+12126delC | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108573953 | |||||
chr6:108574035
|
C | T | 54 | a0001c0002t0001g0178a0001c0002t0001g0184a0001c0002t0002g0149others(51): Show | 54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.621+12206C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574035 | ||||||
chr6:108574140
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.621+12311G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574140 | ||||||
chr6:108574152
|
C | CA | 33 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049others(30): Show | 33 | HG01081.hp1 HG01243.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.621+12343dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108574152 | |||||
chr6:108574168
|
A | G | 1 | a0001c0002t0002g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.621+12339A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574168 | ||||||
chr6:108574168
|
A | T | 1 | a0001c0001t0018g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.621+12339A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574168 | ||||||
chr6:108574170
|
A | G | 19 | a0001c0001t0003g0037a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+12341A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574170 | ||||||
chr6:108574183
|
C | T | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.621+12354C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574183 | ||||||
chr6:108574301
|
A | G | 1 | a0001c0001t0003g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.621+12472A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574301 | ||||||
chr6:108574303
|
G | A | 10 | a0001c0002t0002g0156a0001c0002t0002g0160a0001c0002t0002g0161others(7): Show | 10 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+12474G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574303 | ||||||
chr6:108574386
|
A | G | 1 | a0001c0001t0014g0267 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.621+12557A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574386 | ||||||
chr6:108574589
|
G | A | 33 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0262others(30): Show | 33 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.621+12760G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574589 | ||||||
chr6:108574602
|
C | G | 1 | a0001c0001t0017g0107 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.621+12773C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574602 | ||||||
chr6:108574667
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+12838G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574667 | ||||||
chr6:108574712
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+12883A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574712 | ||||||
chr6:108574772
|
G | A | 1 | a0001c0001t0029g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.621+12943G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574772 | ||||||
chr6:108574864
|
T | G | 1 | a0001c0001t0005g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+13035T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108574864 | ||||||
chr6:108575012
|
A | G | 109 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.621+13183A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575012 | ||||||
chr6:108575025
|
A | G | 2 | a0001c0002t0002g0187a0001c0002t0002g0188 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.621+13196A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575025 | ||||||
chr6:108575126
|
G | T | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+13297G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575126 | ||||||
chr6:108575374
|
T | C | 1 | a0001c0001t0007g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.621+13545T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575374 | ||||||
chr6:108575389
|
AAAAG | A | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0244others(3): Show | 6 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+13564_621+1356 others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108575389 | |||||
chr6:108575609
|
T | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+13780T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575609 | ||||||
chr6:108575661
|
C | A | 1 | a0001c0001t0041g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.621+13832C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575661 | ||||||
chr6:108575789
|
G | A | 267 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.621+13960G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108575789 | ||||||
chr6:108576065
|
T | C | 3 | a0001c0002t0002g0209a0001c0002t0002g0210a0001c0002t0002g0211 | 3 | HG01884.hp2 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.621+14236T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108576065 | ||||||
chr6:108576183
|
A | G | 36 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0262others(33): Show | 36 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.621+14354A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108576183 | ||||||
chr6:108576458
|
G | A | 38 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.621+14629G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108576458 | ||||||
chr6:108576719
|
C | T | 266 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.621+14890C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108576719 | ||||||
chr6:108577202
|
T | TA | 264 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.621+15382dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108577202 | |||||
chr6:108577242
|
A | G | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+15413A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577242 | ||||||
chr6:108577250
|
T | G | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+15421T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577250 | ||||||
chr6:108577260
|
C | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+15431C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577260 | ||||||
chr6:108577262
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.621+15433A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577262 | ||||||
chr6:108577276
|
C | G | 1 | a0001c0002t0002g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.621+15447C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577276 | ||||||
chr6:108577335
|
T | C | 1 | a0001c0002t0002g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.621+15506T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577335 | ||||||
chr6:108577505
|
C | T | 1 | a0001c0001t0003g0223 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621+15676C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577505 | ||||||
chr6:108577869
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+16040G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108577869 | ||||||
chr6:108578341
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.621+16512G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578341 | ||||||
chr6:108578632
|
T | G | 34 | a0001c0001t0002g0258a0001c0001t0003g0037a0001c0001t0003g0262others(31): Show | 34 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.621+16803T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578632 | ||||||
chr6:108578642
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+16813T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578642 | ||||||
chr6:108578854
|
C | T | 11 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(8): Show | 11 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.621+17025C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578854 | ||||||
chr6:108578869
|
G | A | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+17040G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578869 | ||||||
chr6:108578935
|
A | T | 1 | a0001c0001t0003g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.621+17106A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108578935 | ||||||
chr6:108579130
|
TAAAAC | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+17315_621+1731 others(9): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108579130 | |||||
chr6:108579278
|
T | C | 1 | a0001c0001t0010g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.621+17449T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108579278 | ||||||
chr6:108579511
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.621+17682T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108579511 | ||||||
chr6:108579678
|
G | C | 10 | a0001c0001t0002g0258a0001c0001t0004g0001a0001c0001t0004g0002others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+17849G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108579678 | ||||||
chr6:108579736
|
A | T | 1 | a0003c0005t0007g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.621+17907A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108579736 | ||||||
chr6:108579933
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+18104G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108579933 | ||||||
chr6:108580060
|
A | T | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621+18231A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580060 | ||||||
chr6:108580183
|
A | AT | 223 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.621+18377dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108580183 | |||||
chr6:108580183
|
A | ATT | 22 | a0001c0001t0001g0025a0001c0001t0001g0106a0001c0001t0001g0116others(19): Show | 22 | HG01433.hp1 HG02055.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.621+18376_621+1837 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108580183 | |||||
chr6:108580183
|
ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+18369_621+1837 others(13): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108580183 | |||||
chr6:108580443
|
C | T | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.621+18614C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580443 | ||||||
chr6:108580936
|
C | T | 54 | a0001c0002t0001g0178a0001c0002t0001g0184a0001c0002t0002g0149others(51): Show | 54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.621+19107C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580936 | ||||||
chr6:108580953
|
C | T | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.621+19124C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580953 | ||||||
chr6:108580956
|
G | C | 1 | a0001c0002t0036g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.621+19127G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580956 | ||||||
chr6:108580977
|
A | G | 37 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(34): Show | 37 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.621+19148A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108580977 | ||||||
chr6:108581144
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.621+19315G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581144 | ||||||
chr6:108581446
|
A | G | 267 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.621+19617A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581446 | ||||||
chr6:108581472
|
A | G | 1 | a0001c0001t0005g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.621+19643A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581472 | ||||||
chr6:108581648
|
T | G | 4 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0235others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+19819T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581648 | ||||||
chr6:108581779
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+19950A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581779 | ||||||
chr6:108581886
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+20057G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581886 | ||||||
chr6:108581932
|
A | T | 1 | a0001c0002t0002g0176 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.621+20103A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108581932 | ||||||
chr6:108582081
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.621+20252A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108582081 | ||||||
chr6:108582109
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.621+20280C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108582109 | ||||||
chr6:108582118
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.621+20289C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108582118 | ||||||
chr6:108582182
|
C | G | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+20353C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108582182 | ||||||
chr6:108582184
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.621+20355A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108582184 | ||||||
chr6:108583039
|
T | C | 1 | a0001c0001t0006g0245 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.621+21210T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583039 | ||||||
chr6:108583342
|
C | T | 1 | a0001c0002t0021g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.621+21513C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583342 | ||||||
chr6:108583647
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.621+21818A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583647 | ||||||
chr6:108583767
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.621+21938A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583767 | ||||||
chr6:108583932
|
G | GTGA | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+22103_621+2210 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583932 | ||||||
chr6:108583933
|
A | C | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+22104A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583933 | ||||||
chr6:108583934
|
A | C | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+22105A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583934 | ||||||
chr6:108583935
|
G | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+22106G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583935 | ||||||
chr6:108583937
|
T | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+22108T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583937 | ||||||
chr6:108583974
|
C | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+22145C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108583974 | ||||||
chr6:108584062
|
G | A | 1 | a0001c0002t0002g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.621+22233G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584062 | ||||||
chr6:108584378
|
A | AC | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+22549_621+2255 others(5): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584378 | ||||||
chr6:108584477
|
G | A | 109 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.621+22648G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584477 | ||||||
chr6:108584506
|
T | A | 5 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+22677T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584506 | ||||||
chr6:108584657
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.621+22828A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584657 | ||||||
chr6:108584722
|
T | A | 266 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.621+22893T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584722 | ||||||
chr6:108584810
|
A | G | 1 | a0001c0002t0036g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.621+22981A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584810 | ||||||
chr6:108584923
|
A | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+23094A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584923 | ||||||
chr6:108584943
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.621+23114C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584943 | ||||||
chr6:108584997
|
C | T | 97 | a0001c0001t0002g0152a0001c0001t0002g0208a0001c0001t0002g0242others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.621+23168C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108584997 | ||||||
chr6:108585022
|
C | CT | 50 | a0001c0001t0002g0131a0001c0001t0002g0152a0001c0001t0002g0208others(47): Show | 50 | HG00323.hp2 HG01516.hp2 HG01517.hp2 others(47): Show |
intron_variant | MODIFIER | c.621+23223dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTT | 31 | a0001c0001t0001g0034a0001c0001t0003g0265a0001c0001t0003g0268others(28): Show | 31 | HG00140.hp2 HG01123.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.621+23222_621+2322 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTTT | 25 | a0001c0001t0001g0053a0001c0001t0002g0035a0001c0001t0003g0266others(22): Show | 25 | HG01081.hp1 HG02055.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.621+23221_621+2322 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTTTT | 38 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0038others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.621+23220_621+2322 others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTTTTT | 46 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(43): Show | 46 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.621+23219_621+2322 others(9): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTTTTTT | 14 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0093others(11): Show | 14 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.621+23218_621+2322 others(10): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
C | CTTTTTTT | 6 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00735.hp1 HG01884.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+23217_621+2322 others(11): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0002g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.621+23212_621+2322 others(16): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+23211_621+2322 others(17): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585022
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0041g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.621+23210_621+2322 others(18): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108585022 | |||||
chr6:108585065
|
C | T | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+23236C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585065 | ||||||
chr6:108585066
|
G | A | 4 | a0001c0001t0002g0208a0001c0001t0003g0221a0001c0001t0003g0237others(1): Show | 4 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+23237G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585066 | ||||||
chr6:108585143
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+23314G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585143 | ||||||
chr6:108585167
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+23338G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585167 | ||||||
chr6:108585197
|
G | A | 2 | a0001c0001t0003g0150a0001c0001t0003g0226 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.621+23368G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585197 | ||||||
chr6:108585204
|
G | C | 30 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(27): Show | 30 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.621+23375G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585204 | ||||||
chr6:108585233
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.621+23404C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585233 | ||||||
chr6:108585339
|
G | A | 1 | a0001c0001t0009g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.621+23510G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585339 | ||||||
chr6:108585341
|
C | A | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+23512C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585341 | ||||||
chr6:108585509
|
A | G | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+23680A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585509 | ||||||
chr6:108585542
|
G | A | 4 | a0001c0001t0006g0247a0001c0001t0006g0248a0001c0001t0006g0250others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+23713G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585542 | ||||||
chr6:108585662
|
C | T | 1 | a0001c0001t0003g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.621+23833C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585662 | ||||||
chr6:108585810
|
A | G | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621+23981A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108585810 | ||||||
chr6:108586072
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+24243C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586072 | ||||||
chr6:108586319
|
G | A | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+24490G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586319 | ||||||
chr6:108586387
|
C | T | 2 | a0001c0002t0002g0186a0001c0002t0003g0167 | 2 | NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.621+24558C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586387 | ||||||
chr6:108586399
|
G | A | 1 | a0001c0001t0033g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.621+24570G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586399 | ||||||
chr6:108586465
|
GTATC | G | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+24640_621+2464 others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586465 | |||||
chr6:108586508
|
G | T | 1 | a0001c0001t0008g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.621+24679G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586508 | ||||||
chr6:108586936
|
A | ATAT | 16 | a0001c0001t0001g0074a0001c0001t0002g0132a0001c0001t0003g0195others(13): Show | 16 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.621+25157_621+2515 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
A | ATATTAT | 7 | a0001c0001t0003g0216a0001c0001t0005g0124a0001c0001t0005g0127others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+25154_621+2515 others(10): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATAT | A | 58 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.621+25157_621+2515 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTAT | A | 72 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0060others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.621+25154_621+2515 others(10): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTATT others(2): Show |
A | 66 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0038others(63): Show | 66 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.621+25151_621+2515 others(13): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTATT others(5): Show |
A | 14 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0003g0016others(11): Show | 14 | HG00099.hp2 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.621+25148_621+2515 others(16): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTATT others(8): Show |
A | 7 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0004others(4): Show | 7 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+25145_621+2515 others(19): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTATT others(11): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.621+25142_621+2515 others(22): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586936
|
ATATTATT others(14): Show |
A | 3 | a0001c0001t0001g0025a0001c0001t0001g0090a0001c0001t0001g0252 | 3 | HG02293.hp1 HG02293.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.621+25139_621+2515 others(25): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108586936 | |||||
chr6:108586956
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+25127A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108586956 | ||||||
chr6:108587017
|
C | T | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+25188C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587017 | ||||||
chr6:108587193
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.621+25364T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587193 | ||||||
chr6:108587193
|
T | G | 1 | a0001c0001t0008g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.621+25364T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587193 | ||||||
chr6:108587315
|
G | T | 108 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.621+25486G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587315 | ||||||
chr6:108587370
|
C | A | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+25541C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587370 | ||||||
chr6:108587400
|
C | T | 1 | a0001c0002t0002g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.621+25571C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587400 | ||||||
chr6:108587489
|
A | C | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.621+25660A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587489 | ||||||
chr6:108587550
|
C | T | 1 | a0001c0001t0018g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.621+25721C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587550 | ||||||
chr6:108587632
|
T | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+25803T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587632 | ||||||
chr6:108587850
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.621+26021A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587850 | ||||||
chr6:108587887
|
G | A | 1 | a0001c0001t0008g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.621+26058G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108587887 | ||||||
chr6:108588064
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+26235A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108588064 | ||||||
chr6:108588080
|
C | CTT | 7 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+26253_621+2625 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108588080 | |||||
chr6:108588248
|
C | T | 1 | a0001c0001t0006g0245 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.621+26419C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108588248 | ||||||
chr6:108588315
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+26486C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108588315 | ||||||
chr6:108588476
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.621+26647G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108588476 | ||||||
chr6:108588830
|
G | C | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.621+27001G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108588830 | ||||||
chr6:108589082
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0063others(5): Show | 8 | HG00621.hp1 HG02027.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.621+27253G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589082 | ||||||
chr6:108589159
|
T | G | 1 | a0001c0002t0002g0228 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.621+27330T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589159 | ||||||
chr6:108589332
|
C | T | 10 | a0001c0001t0002g0258a0001c0001t0004g0001a0001c0001t0004g0002others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+27503C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589332 | ||||||
chr6:108589378
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+27549C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589378 | ||||||
chr6:108589586
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+27757C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589586 | ||||||
chr6:108589619
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.621+27790G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589619 | ||||||
chr6:108589868
|
A | C | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+28039A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589868 | ||||||
chr6:108589953
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0014g0047 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.621+28124C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108589953 | ||||||
chr6:108590148
|
T | C | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.621+28319T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108590148 | ||||||
chr6:108590770
|
A | G | 34 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(31): Show | 34 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.621+28941A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108590770 | ||||||
chr6:108590817
|
C | G | 10 | a0001c0001t0002g0258a0001c0001t0004g0001a0001c0001t0004g0002others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+28988C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108590817 | ||||||
chr6:108590889
|
C | T | 3 | a0001c0002t0002g0209a0001c0002t0002g0210a0001c0002t0002g0211 | 3 | HG01884.hp2 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.621+29060C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108590889 | ||||||
chr6:108591140
|
A | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.621+29311A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591140 | ||||||
chr6:108591279
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.621+29450A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591279 | ||||||
chr6:108591329
|
A | G | 1 | a0001c0003t0003g0225 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.621+29500A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591329 | ||||||
chr6:108591440
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621+29611A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591440 | ||||||
chr6:108591485
|
C | G | 4 | a0001c0001t0003g0197a0001c0001t0003g0205a0001c0001t0003g0206others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+29656C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591485 | ||||||
chr6:108591877
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+30048C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591877 | ||||||
chr6:108591886
|
TA | T | 145 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0093others(142): Show | 145 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.621+30071delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108591886 | |||||
chr6:108591886
|
TAA | T | 108 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.621+30070_621+3007 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108591886 | |||||
chr6:108591998
|
T | C | 20 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0058others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+30169T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108591998 | ||||||
chr6:108592302
|
A | G | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621+30473A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108592302 | ||||||
chr6:108592362
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.621+30533G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108592362 | ||||||
chr6:108592667
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.621+30838T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108592667 | ||||||
chr6:108593058
|
A | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+31229A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593058 | ||||||
chr6:108593164
|
GAGGATTA others(67): Show |
G | 1 | a0001c0001t0034g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.621+31338_621+3141 others(78): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593164 | |||||
chr6:108593356
|
A | T | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.621+31527A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593356 | ||||||
chr6:108593392
|
C | CT | 5 | a0001c0001t0020g0018a0001c0001t0020g0019a0002c0004t0001g0012others(2): Show | 5 | HG00735.hp2 HG01074.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+31574dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593392 | |||||
chr6:108593416
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0002g0130a0001c0001t0002g0131others(5): Show | 8 | HG01517.hp1 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+31587C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593416 | ||||||
chr6:108593578
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.621+31749A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593578 | ||||||
chr6:108593634
|
T | A | 1 | a0001c0001t0044g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.621+31805T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593634 | ||||||
chr6:108593712
|
C | CT | 52 | a0001c0001t0001g0039a0001c0001t0001g0093a0001c0001t0001g0111others(49): Show | 52 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.621+31905dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593712 | |||||
chr6:108593712
|
C | CTT | 51 | a0001c0001t0001g0033a0001c0001t0002g0242a0001c0001t0002g0243others(48): Show | 51 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.621+31904_621+3190 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593712 | |||||
chr6:108593712
|
C | CTTT | 7 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0180others(4): Show | 7 | HG00735.hp2 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+31903_621+3190 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593712 | |||||
chr6:108593712
|
CT | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0096a0001c0001t0004g0005others(6): Show | 9 | HG00323.hp1 HG00323.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+31905delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108593712 | |||||
chr6:108593715
|
T | C | 1 | a0001c0001t0007g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.621+31886T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593715 | ||||||
chr6:108593754
|
T | C | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.621+31925T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593754 | ||||||
chr6:108593789
|
T | C | 1 | a0001c0001t0018g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.621+31960T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593789 | ||||||
chr6:108593852
|
G | GCT | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+32023_621+3202 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593852 | ||||||
chr6:108593853
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+32024A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593853 | ||||||
chr6:108593855
|
T | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+32026T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593855 | ||||||
chr6:108593856
|
A | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+32027A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108593856 | ||||||
chr6:108594008
|
C | G | 1 | a0001c0002t0002g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.621+32179C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108594008 | ||||||
chr6:108594271
|
T | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+32442T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108594271 | ||||||
chr6:108594942
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+33113G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108594942 | ||||||
chr6:108594944
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+33115T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108594944 | ||||||
chr6:108595176
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+33347G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595176 | ||||||
chr6:108595203
|
G | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018 | 3 | HG03041.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+33374G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595203 | ||||||
chr6:108595222
|
G | A | 12 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(9): Show | 12 | HG01884.hp1 HG02922.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.621+33393G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595222 | ||||||
chr6:108595370
|
T | C | 55 | a0001c0001t0001g0033a0001c0002t0001g0178a0001c0002t0001g0184others(52): Show | 55 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.621+33541T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595370 | ||||||
chr6:108595444
|
A | G | 2 | a0001c0001t0003g0266a0001c0001t0003g0270 | 2 | HG02080.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.621+33615A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595444 | ||||||
chr6:108595561
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.621+33732T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595561 | ||||||
chr6:108595585
|
T | A | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621+33756T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595585 | ||||||
chr6:108595866
|
G | A | 20 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+34037G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595866 | ||||||
chr6:108595993
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.621+34164A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108595993 | ||||||
chr6:108596169
|
C | A | 4 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(1): Show | 4 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+34340C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596169 | ||||||
chr6:108596176
|
C | A | 4 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(1): Show | 4 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+34347C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596176 | ||||||
chr6:108596206
|
G | A | 1 | a0001c0001t0007g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+34377G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596206 | ||||||
chr6:108596382
|
G | GA | 20 | a0001c0001t0001g0102a0001c0001t0003g0221a0001c0001t0003g0237others(17): Show | 20 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.621+34577dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108596382 | |||||
chr6:108596382
|
GA | G | 42 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0040others(39): Show | 42 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.621+34577delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108596382 | |||||
chr6:108596382
|
GAA | G | 12 | a0001c0001t0003g0017a0001c0001t0003g0263a0001c0001t0003g0264others(9): Show | 12 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.621+34576_621+3457 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108596382 | |||||
chr6:108596485
|
T | A | 37 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(34): Show | 37 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.621+34656T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596485 | ||||||
chr6:108596548
|
G | A | 1 | a0001c0001t0029g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.621+34719G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596548 | ||||||
chr6:108596580
|
G | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+34751G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596580 | ||||||
chr6:108596798
|
C | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+34969C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596798 | ||||||
chr6:108596861
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.621+35032A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108596861 | ||||||
chr6:108597047
|
G | T | 1 | a0001c0001t0028g0277 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.621+35218G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597047 | ||||||
chr6:108597051
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+35222G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597051 | ||||||
chr6:108597340
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0027g0261 | 3 | HG00323.hp2 HG02071.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.621+35511G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597340 | ||||||
chr6:108597471
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.621+35642T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597471 | ||||||
chr6:108597475
|
T | A | 1 | a0001c0001t0023g0119 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.621+35646T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597475 | ||||||
chr6:108597713
|
T | A | 1 | a0001c0001t0026g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+35884T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108597713 | ||||||
chr6:108598443
|
A | G | 20 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+36614A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598443 | ||||||
chr6:108598524
|
G | A | 28 | a0001c0002t0002g0149a0001c0002t0002g0156a0001c0002t0002g0158others(25): Show | 28 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.621+36695G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598524 | ||||||
chr6:108598540
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.621+36711A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598540 | ||||||
chr6:108598575
|
C | T | 1 | a0001c0006t0001g0080 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.621+36746C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598575 | ||||||
chr6:108598767
|
A | G | 20 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+36938A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598767 | ||||||
chr6:108598905
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+37076C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108598905 | ||||||
chr6:108599017
|
T | C | 1 | a0001c0002t0002g0183 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.621+37188T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108599017 | ||||||
chr6:108599386
|
A | G | 265 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.621+37557A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108599386 | ||||||
chr6:108599624
|
A | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+37795A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108599624 | ||||||
chr6:108599711
|
G | A | 3 | a0001c0001t0007g0029a0001c0001t0007g0030a0003c0005t0007g0031 | 3 | HG01081.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.621+37882G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108599711 | ||||||
chr6:108599954
|
A | G | 38 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.621+38125A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108599954 | ||||||
chr6:108600068
|
C | A | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.621+38239C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600068 | ||||||
chr6:108600159
|
T | C | 2 | a0001c0001t0003g0215a0001c0001t0003g0227 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.621+38330T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600159 | ||||||
chr6:108600184
|
G | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+38355G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600184 | ||||||
chr6:108600282
|
C | T | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+38453C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600282 | ||||||
chr6:108600310
|
C | T | 3 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0028g0277 | 3 | HG02698.hp1 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.621+38481C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600310 | ||||||
chr6:108600344
|
A | G | 267 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.621+38515A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600344 | ||||||
chr6:108600376
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.621+38547C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600376 | ||||||
chr6:108600546
|
C | CA | 24 | a0001c0001t0002g0244a0001c0001t0003g0221a0001c0001t0003g0237others(21): Show | 24 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.621+38744dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108600546 | |||||
chr6:108600546
|
CA | C | 99 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.621+38744delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108600546 | |||||
chr6:108600546
|
CAA | C | 28 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0096others(25): Show | 28 | HG00280.hp1 HG00639.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.621+38743_621+3874 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108600546 | |||||
chr6:108600643
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+38814A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600643 | ||||||
chr6:108600760
|
G | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+38931G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600760 | ||||||
chr6:108600990
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.621+39161T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108600990 | ||||||
chr6:108601010
|
A | G | 2 | a0001c0001t0004g0004a0001c0001t0004g0007 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.621+39181A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601010 | ||||||
chr6:108601129
|
T | A | 38 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.621+39300T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601129 | ||||||
chr6:108601174
|
A | AT | 11 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(8): Show | 11 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.621+39356dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108601174 | |||||
chr6:108601222
|
C | T | 4 | a0001c0001t0002g0258a0002c0004t0001g0012a0002c0004t0001g0013others(1): Show | 4 | HG00735.hp2 HG01074.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+39393C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601222 | ||||||
chr6:108601264
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0008g0100others(1): Show | 4 | HG02165.hp2 NA18981.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+39435G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601264 | ||||||
chr6:108601265
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+39436G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601265 | ||||||
chr6:108601423
|
C | T | 20 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+39594C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601423 | ||||||
chr6:108601606
|
C | A | 1 | a0001c0002t0002g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.621+39777C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601606 | ||||||
chr6:108601706
|
T | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0263 | 2 | HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.621+39877T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601706 | ||||||
chr6:108601721
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0020g0018others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+39892T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108601721 | ||||||
chr6:108602322
|
T | C | 19 | a0001c0001t0003g0037a0001c0001t0003g0262a0001c0001t0003g0263others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+40493T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108602322 | ||||||
chr6:108602479
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+40650G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108602479 | ||||||
chr6:108602701
|
A | G | 1 | a0001c0002t0002g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.621+40872A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108602701 | ||||||
chr6:108602827
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.621+40998A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108602827 | ||||||
chr6:108603067
|
A | G | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+41238A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603067 | ||||||
chr6:108603287
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+41458C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603287 | ||||||
chr6:108603363
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.621+41534T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603363 | ||||||
chr6:108603455
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+41626C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603455 | ||||||
chr6:108603531
|
T | C | 1 | a0001c0001t0005g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+41702T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603531 | ||||||
chr6:108603586
|
A | G | 30 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0037others(27): Show | 30 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.621+41757A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603586 | ||||||
chr6:108603776
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+41947A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603776 | ||||||
chr6:108603963
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.621+42134A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108603963 | ||||||
chr6:108604060
|
C | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+42231C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108604060 | ||||||
chr6:108604724
|
T | G | 1 | a0001c0001t0003g0276 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.621+42895T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108604724 | ||||||
chr6:108604822
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.621+42993C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108604822 | ||||||
chr6:108604928
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.621+43099T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108604928 | ||||||
chr6:108605058
|
GAGATAAA others(3): Show |
G | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621+43232_621+4324 others(14): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108605058 | |||||
chr6:108605100
|
C | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+43271C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605100 | ||||||
chr6:108605123
|
C | CT | 29 | a0001c0001t0002g0258a0001c0001t0003g0017a0001c0001t0003g0262others(26): Show | 29 | HG00323.hp2 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.621+43303dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108605123 | |||||
chr6:108605293
|
A | G | 109 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.621+43464A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605293 | ||||||
chr6:108605408
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.621+43579C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605408 | ||||||
chr6:108605526
|
C | G | 2 | a0001c0002t0002g0233a0001c0002t0013g0234 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.621+43697C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605526 | ||||||
chr6:108605582
|
A | G | 3 | a0001c0002t0002g0161a0001c0002t0002g0230a0001c0002t0002g0231 | 3 | HG01257.hp1 HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.621+43753A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605582 | ||||||
chr6:108605594
|
A | G | 1 | a0001c0002t0002g0166 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.621+43765A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605594 | ||||||
chr6:108605782
|
A | G | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.621+43953A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108605782 | ||||||
chr6:108606286
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.621+44457A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606286 | ||||||
chr6:108606589
|
TTTC | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+44768_621+4477 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108606589 | |||||
chr6:108606638
|
C | T | 56 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0002t0001g0178others(53): Show | 56 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.621+44809C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606638 | ||||||
chr6:108606639
|
A | G | 99 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.621+44810A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606639 | ||||||
chr6:108606665
|
C | T | 1 | a0001c0001t0003g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.621+44836C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606665 | ||||||
chr6:108606755
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.621+44926C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606755 | ||||||
chr6:108606968
|
G | A | 54 | a0001c0002t0001g0178a0001c0002t0001g0184a0001c0002t0002g0149others(51): Show | 54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.621+45139G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108606968 | ||||||
chr6:108607039
|
T | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+45210T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607039 | ||||||
chr6:108607169
|
CA | C | 8 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(5): Show | 8 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+45341delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607169 | ||||||
chr6:108607177
|
C | T | 7 | a0001c0001t0003g0037a0001c0001t0003g0272a0001c0001t0003g0273others(4): Show | 7 | HG02155.hp1 HG02698.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+45348C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607177 | ||||||
chr6:108607247
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG01943.hp2 NA18956.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.621+45418T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607247 | ||||||
chr6:108607361
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.621+45532A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607361 | ||||||
chr6:108607447
|
C | CA | 41 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(38): Show | 41 | HG00323.hp2 HG01243.hp1 HG01943.hp2 others(38): Show |
intron_variant | MODIFIER | c.621+45636dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108607447 | |||||
chr6:108607472
|
G | A | 39 | a0001c0001t0002g0035a0001c0001t0002g0258a0001c0001t0003g0017others(36): Show | 39 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.621+45643G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607472 | ||||||
chr6:108607626
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.621+45797A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607626 | ||||||
chr6:108607747
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.621+45918G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607747 | ||||||
chr6:108607955
|
A | G | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+46126A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108607955 | ||||||
chr6:108608872
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.621+47043C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108608872 | ||||||
chr6:108608886
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.621+47057C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108608886 | ||||||
chr6:108609066
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.621+47237G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609066 | ||||||
chr6:108609334
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.621+47505T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609334 | ||||||
chr6:108609430
|
T | C | 265 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.621+47601T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609430 | ||||||
chr6:108609507
|
C | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+47678C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609507 | ||||||
chr6:108609707
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+47878C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609707 | ||||||
chr6:108609914
|
G | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+48085G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108609914 | ||||||
chr6:108610801
|
T | C | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+48972T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108610801 | ||||||
chr6:108610935
|
C | G | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+49106C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108610935 | ||||||
chr6:108610957
|
C | T | 263 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.621+49128C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108610957 | ||||||
chr6:108611005
|
C | A | 15 | a0001c0001t0003g0134a0001c0001t0004g0001a0001c0001t0004g0002others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.621+49176C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611005 | ||||||
chr6:108611098
|
AT | A | 86 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0001t0001g0072others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.621+49271delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108611098 | |||||
chr6:108611151
|
G | A | 3 | a0001c0001t0003g0203a0001c0001t0003g0207a0004c0008t0001g0256 | 3 | HG02071.hp1 NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.621+49322G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611151 | ||||||
chr6:108611264
|
C | T | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+49435C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611264 | ||||||
chr6:108611426
|
TA | T | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.621+49598delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611426 | ||||||
chr6:108611438
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | NA18940.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.621+49609C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611438 | ||||||
chr6:108611512
|
C | A | 10 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+49683C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611512 | ||||||
chr6:108611696
|
C | CT | 6 | a0001c0001t0001g0065a0001c0001t0002g0208a0001c0001t0008g0084others(3): Show | 6 | HG03453.hp1 HG03486.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+49881dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108611696 | |||||
chr6:108611711
|
A | T | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.621+49882A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611711 | ||||||
chr6:108611851
|
A | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.621+50022A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611851 | ||||||
chr6:108611950
|
T | C | 1 | a0001c0001t0006g0010 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.621+50121T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108611950 | ||||||
chr6:108612405
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+50576C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612405 | ||||||
chr6:108612408
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.621+50579G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612408 | ||||||
chr6:108612454
|
C | A | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.621+50625C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612454 | ||||||
chr6:108612466
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.621+50637G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612466 | ||||||
chr6:108612604
|
C | G | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.621+50775C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612604 | ||||||
chr6:108612605
|
G | A | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.621+50776G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612605 | ||||||
chr6:108612623
|
T | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.621+50794T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612623 | ||||||
chr6:108612650
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-50805A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612650 | ||||||
chr6:108612691
|
T | A | 5 | a0001c0001t0003g0203a0001c0001t0003g0207a0001c0002t0002g0209others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-50764T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612691 | ||||||
chr6:108612692
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.622-50763A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108612692 | ||||||
chr6:108613196
|
T | G | 1 | a0001c0001t0003g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.622-50259T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613196 | ||||||
chr6:108613258
|
C | T | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.622-50197C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613258 | ||||||
chr6:108613361
|
GT | G | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.622-50087delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108613361 | |||||
chr6:108613493
|
T | A | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622-49962T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613493 | ||||||
chr6:108613597
|
A | G | 7 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141others(4): Show | 7 | HG01884.hp1 HG02135.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-49858A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613597 | ||||||
chr6:108613672
|
G | A | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-49783G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613672 | ||||||
chr6:108613695
|
C | T | 7 | a0001c0001t0003g0017a0001c0001t0013g0020a0001c0001t0013g0021others(4): Show | 7 | HG02145.hp1 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-49760C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613695 | ||||||
chr6:108613704
|
C | T | 2 | a0001c0002t0002g0193a0001c0002t0010g0192 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.622-49751C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613704 | ||||||
chr6:108613762
|
C | A | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-49693C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613762 | ||||||
chr6:108613929
|
A | G | 265 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.622-49526A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613929 | ||||||
chr6:108613966
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0001g0111others(1): Show | 4 | NA18940.hp2 NA18966.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-49489G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108613966 | ||||||
chr6:108614188
|
G | T | 1 | a0001c0001t0011g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.622-49267G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614188 | ||||||
chr6:108614374
|
A | T | 2 | a0001c0001t0003g0016a0001c0001t0014g0047 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.622-49081A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614374 | ||||||
chr6:108614513
|
A | G | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.622-48942A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614513 | ||||||
chr6:108614518
|
C | T | 1 | a0001c0001t0041g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-48937C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614518 | ||||||
chr6:108614691
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.622-48764G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614691 | ||||||
chr6:108614712
|
G | T | 71 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0002g0208others(68): Show | 71 | HG00140.hp2 HG01074.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.622-48743G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614712 | ||||||
chr6:108614713
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.622-48742T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614713 | ||||||
chr6:108614722
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-48733G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108614722 | ||||||
chr6:108615093
|
G | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-48362G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615093 | ||||||
chr6:108615232
|
G | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-48223G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615232 | ||||||
chr6:108615392
|
C | A | 1 | a0001c0001t0030g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.622-48063C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615392 | ||||||
chr6:108615400
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0014g0047 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.622-48055C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615400 | ||||||
chr6:108615404
|
CTT | C | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-48050_622-4804 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615404 | ||||||
chr6:108615606
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622-47849T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615606 | ||||||
chr6:108615620
|
A | T | 1 | a0001c0001t0003g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.622-47835A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615620 | ||||||
chr6:108615997
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.622-47458T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108615997 | ||||||
chr6:108616156
|
G | GT | 9 | a0001c0001t0002g0132a0001c0001t0003g0265a0001c0001t0006g0250others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-47273dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108616156 | |||||
chr6:108616156
|
GT | G | 147 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.622-47273delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108616156 | |||||
chr6:108616156
|
GTT | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0085others(7): Show | 10 | HG01074.hp2 HG01516.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-47274_622-4727 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108616156 | |||||
chr6:108616161
|
T | C | 18 | a0001c0001t0003g0151a0001c0001t0003g0153a0001c0001t0003g0196others(15): Show | 18 | HG00438.hp2 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.622-47294T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616161 | ||||||
chr6:108616182
|
TG | T | 7 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-47272delG | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616182 | ||||||
chr6:108616183
|
G | T | 2 | a0001c0001t0004g0005a0001c0001t0004g0009 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.622-47272G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616183 | ||||||
chr6:108616199
|
C | T | 2 | a0001c0001t0003g0264a0001c0001t0003g0265 | 2 | HG02071.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.622-47256C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616199 | ||||||
chr6:108616225
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-47230C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616225 | ||||||
chr6:108616408
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.622-47047G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616408 | ||||||
chr6:108616554
|
C | A | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-46901C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616554 | ||||||
chr6:108616670
|
CA | C | 27 | a0001c0002t0002g0149a0001c0002t0002g0156a0001c0002t0002g0158others(24): Show | 27 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.622-46782delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108616670 | |||||
chr6:108616725
|
C | T | 1 | a0001c0002t0002g0183 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622-46730C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616725 | ||||||
chr6:108616785
|
T | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0021g0015 | 3 | HG03098.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.622-46670T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108616785 | ||||||
chr6:108617109
|
G | A | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-46346G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617109 | ||||||
chr6:108617246
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-46209C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617246 | ||||||
chr6:108617598
|
T | G | 1 | a0001c0001t0004g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.622-45857T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617598 | ||||||
chr6:108617626
|
G | GT | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-45823dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108617626 | |||||
chr6:108617773
|
A | G | 3 | a0001c0001t0003g0134a0001c0001t0003g0135a0001c0003t0016g0240 | 3 | HG03453.hp2 HG03471.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.622-45682A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617773 | ||||||
chr6:108617785
|
C | T | 1 | a0001c0002t0010g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622-45670C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617785 | ||||||
chr6:108617812
|
G | A | 29 | a0001c0002t0002g0149a0001c0002t0002g0156a0001c0002t0002g0158others(26): Show | 29 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.622-45643G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617812 | ||||||
chr6:108617814
|
G | GCTT | 29 | a0001c0002t0002g0149a0001c0002t0002g0156a0001c0002t0002g0158others(26): Show | 29 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.622-45640_622-4563 others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108617814 | |||||
chr6:108617850
|
A | T | 1 | a0001c0001t0008g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.622-45605A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617850 | ||||||
chr6:108617880
|
C | G | 34 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(31): Show | 34 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.622-45575C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108617880 | ||||||
chr6:108618094
|
T | C | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.622-45361T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618094 | ||||||
chr6:108618100
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-45355G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618100 | ||||||
chr6:108618260
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.622-45195C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618260 | ||||||
chr6:108618541
|
C | G | 7 | a0001c0001t0003g0017a0001c0001t0013g0020a0001c0001t0013g0021others(4): Show | 7 | HG02145.hp1 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-44914C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618541 | ||||||
chr6:108618668
|
A | C | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-44787A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618668 | ||||||
chr6:108618860
|
C | A | 1 | a0001c0002t0002g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.622-44595C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108618860 | ||||||
chr6:108619077
|
T | C | 53 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(50): Show | 53 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.622-44378T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108619077 | ||||||
chr6:108619167
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.622-44288C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108619167 | ||||||
chr6:108619621
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0008g0095a0001c0001t0042g0043 | 3 | HG01255.hp2 HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.622-43834C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108619621 | ||||||
chr6:108620190
|
A | G | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-43265A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620190 | ||||||
chr6:108620218
|
A | G | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-43237A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620218 | ||||||
chr6:108620233
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.622-43222A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620233 | ||||||
chr6:108620265
|
A | G | 48 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(45): Show | 48 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.622-43190A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620265 | ||||||
chr6:108620289
|
A | C | 2 | a0001c0001t0003g0262a0001c0001t0003g0263 | 2 | HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.622-43166A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620289 | ||||||
chr6:108620515
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.622-42940A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620515 | ||||||
chr6:108620592
|
C | T | 2 | a0001c0001t0017g0107a0001c0001t0031g0068 | 2 | HG00673.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.622-42863C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620592 | ||||||
chr6:108620609
|
A | G | 1 | a0001c0001t0020g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.622-42846A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620609 | ||||||
chr6:108620613
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-42842G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620613 | ||||||
chr6:108620630
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-42825T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108620630 | ||||||
chr6:108620671
|
ATTTTC | A | 117 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.622-42779_622-4277 others(9): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108620671 | |||||
chr6:108621129
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0003g0224 | 2 | HG01975.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.622-42326G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108621129 | ||||||
chr6:108621135
|
T | C | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-42320T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108621135 | ||||||
chr6:108621220
|
G | A | 3 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141 | 3 | HG02135.hp2 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.622-42235G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108621220 | ||||||
chr6:108621447
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-42008G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108621447 | ||||||
chr6:108621541
|
GT | G | 52 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(49): Show | 52 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.622-41905delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108621541 | |||||
chr6:108621745
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.622-41710T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108621745 | ||||||
chr6:108622043
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-41412G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622043 | ||||||
chr6:108622113
|
G | T | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-41342G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622113 | ||||||
chr6:108622216
|
G | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-41239G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622216 | ||||||
chr6:108622221
|
T | A | 1 | a0001c0001t0003g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.622-41234T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622221 | ||||||
chr6:108622256
|
C | CA | 74 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0086others(71): Show | 74 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(71): Show |
intron_variant | MODIFIER | c.622-41175dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108622256 | |||||
chr6:108622256
|
C | CAA | 7 | a0001c0001t0001g0116a0001c0001t0003g0274a0001c0002t0002g0165others(4): Show | 7 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-41176_622-4117 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108622256 | |||||
chr6:108622256
|
CA | C | 6 | a0001c0001t0001g0039a0001c0001t0003g0150a0001c0001t0003g0215others(3): Show | 6 | HG01943.hp2 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-41175delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108622256 | |||||
chr6:108622287
|
G | T | 2 | a0001c0001t0011g0145a0001c0001t0011g0146 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.622-41168G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622287 | ||||||
chr6:108622856
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0114 | 3 | HG00639.hp2 HG01081.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622-40599G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622856 | ||||||
chr6:108622931
|
G | GA | 10 | a0001c0001t0001g0033a0001c0001t0001g0093a0001c0001t0003g0155others(7): Show | 10 | HG02055.hp2 HG02080.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-40506dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108622931 | |||||
chr6:108622962
|
C | T | 170 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.622-40493C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108622962 | ||||||
chr6:108623387
|
T | A | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-40068T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108623387 | ||||||
chr6:108623402
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.622-40053C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108623402 | ||||||
chr6:108623815
|
C | G | 2 | a0001c0002t0002g0236a0001c0002t0002g0255 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.622-39640C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108623815 | ||||||
chr6:108623904
|
G | A | 54 | a0001c0001t0002g0035a0001c0001t0002g0258a0001c0002t0002g0149others(51): Show | 54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.622-39551G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108623904 | ||||||
chr6:108623969
|
T | C | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-39486T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108623969 | ||||||
chr6:108624167
|
A | C | 119 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.622-39288A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108624167 | ||||||
chr6:108624266
|
C | G | 2 | a0001c0001t0007g0109a0001c0001t0007g0110 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-39189C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108624266 | ||||||
chr6:108624312
|
T | TA | 6 | a0001c0001t0001g0086a0001c0001t0003g0017a0001c0001t0020g0018others(3): Show | 6 | HG02145.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.622-39130dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108624312 | |||||
chr6:108624312
|
TA | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-39130delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108624312 | |||||
chr6:108624403
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.622-39052T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108624403 | ||||||
chr6:108624726
|
T | G | 2 | a0001c0001t0003g0017a0001c0003t0016g0240 | 2 | HG02145.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.622-38729T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108624726 | ||||||
chr6:108624933
|
T | G | 1 | a0001c0001t0033g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.622-38522T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108624933 | ||||||
chr6:108625123
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.622-38332T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625123 | ||||||
chr6:108625180
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.622-38275A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625180 | ||||||
chr6:108625287
|
T | C | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.622-38168T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625287 | ||||||
chr6:108625355
|
C | T | 1 | a0001c0002t0002g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.622-38100C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625355 | ||||||
chr6:108625837
|
A | G | 2 | a0001c0001t0003g0017a0001c0003t0016g0240 | 2 | HG02145.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.622-37618A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625837 | ||||||
chr6:108625944
|
G | C | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-37511G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108625944 | ||||||
chr6:108626008
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | NA18940.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.622-37447T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626008 | ||||||
chr6:108626380
|
G | T | 1 | a0001c0001t0003g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.622-37075G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626380 | ||||||
chr6:108626593
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.622-36862T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626593 | ||||||
chr6:108626617
|
C | CT | 248 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.622-36828dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108626617 | |||||
chr6:108626705
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-36750G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626705 | ||||||
chr6:108626821
|
G | A | 1 | a0001c0001t0005g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.622-36634G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626821 | ||||||
chr6:108626988
|
T | G | 1 | a0001c0001t0003g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.622-36467T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108626988 | ||||||
chr6:108627027
|
G | A | 1 | a0001c0001t0043g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.622-36428G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627027 | ||||||
chr6:108627092
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0008g0095a0001c0001t0042g0043 | 3 | HG01255.hp2 HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.622-36363C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627092 | ||||||
chr6:108627138
|
T | A | 250 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.622-36317T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627138 | ||||||
chr6:108627711
|
A | C | 1 | a0001c0001t0003g0266 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.622-35744A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627711 | ||||||
chr6:108627899
|
G | A | 19 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(16): Show | 19 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.622-35556G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627899 | ||||||
chr6:108627924
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0008g0084 | 2 | NA18953.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.622-35531T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627924 | ||||||
chr6:108627959
|
A | C | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622-35496A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108627959 | ||||||
chr6:108628074
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG01981.hp2 HG02258.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-35381G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108628074 | ||||||
chr6:108628123
|
G | GA | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-35331dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108628123 | |||||
chr6:108628631
|
G | A | 10 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(7): Show | 10 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-34824G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108628631 | ||||||
chr6:108628642
|
A | G | 16 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-34813A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108628642 | ||||||
chr6:108629082
|
G | A | 3 | a0001c0001t0003g0151a0001c0001t0003g0198a0001c0001t0003g0200 | 3 | NA18954.hp2 NA18983.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.622-34373G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629082 | ||||||
chr6:108629117
|
A | C | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-34338A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629117 | ||||||
chr6:108629259
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.622-34196C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629259 | ||||||
chr6:108629336
|
G | GGGTTGTG others(8): Show |
2 | a0001c0001t0003g0264a0001c0001t0003g0265 | 2 | HG02071.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.622-34116_622-3410 others(19): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108629336 | |||||
chr6:108629640
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-33815G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629640 | ||||||
chr6:108629729
|
G | A | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-33726G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629729 | ||||||
chr6:108629751
|
A | C | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-33704A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629751 | ||||||
chr6:108629826
|
T | C | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-33629T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629826 | ||||||
chr6:108629992
|
C | T | 1 | a0001c0001t0003g0151 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.622-33463C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108629992 | ||||||
chr6:108630102
|
C | T | 3 | a0001c0001t0003g0151a0001c0001t0003g0198a0001c0001t0003g0200 | 3 | NA18954.hp2 NA18983.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.622-33353C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630102 | ||||||
chr6:108630184
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.622-33271C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630184 | ||||||
chr6:108630275
|
C | T | 1 | a0001c0001t0011g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.622-33180C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630275 | ||||||
chr6:108630395
|
T | G | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-33060T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630395 | ||||||
chr6:108630452
|
T | C | 81 | a0001c0001t0001g0033a0001c0001t0001g0098a0001c0001t0002g0035others(78): Show | 81 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(78): Show |
intron_variant | MODIFIER | c.622-33003T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630452 | ||||||
chr6:108630673
|
C | G | 20 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.622-32782C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630673 | ||||||
chr6:108630765
|
T | A | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-32690T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108630765 | ||||||
chr6:108631012
|
C | T | 2 | a0001c0001t0004g0004a0001c0001t0004g0007 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.622-32443C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108631012 | ||||||
chr6:108631134
|
G | A | 57 | a0001c0001t0001g0033a0001c0001t0002g0035a0001c0001t0002g0242others(54): Show | 57 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.622-32321G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108631134 | ||||||
chr6:108631475
|
T | C | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-31980T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108631475 | ||||||
chr6:108631502
|
T | C | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-31953T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108631502 | ||||||
chr6:108631876
|
T | C | 1 | a0001c0001t0011g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.622-31579T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108631876 | ||||||
chr6:108632206
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.622-31249A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632206 | ||||||
chr6:108632433
|
A | G | 10 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(7): Show | 10 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-31022A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632433 | ||||||
chr6:108632595
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-30860C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632595 | ||||||
chr6:108632609
|
G | T | 1 | a0001c0002t0021g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622-30846G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632609 | ||||||
chr6:108632611
|
CAGTG | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-30841_622-3083 others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108632611 | |||||
chr6:108632666
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.622-30789A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632666 | ||||||
chr6:108632676
|
T | C | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-30779T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632676 | ||||||
chr6:108632772
|
A | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0058others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.622-30683A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108632772 | ||||||
chr6:108633237
|
A | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-30218A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633237 | ||||||
chr6:108633355
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.622-30100T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633355 | ||||||
chr6:108633516
|
G | A | 15 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.622-29939G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633516 | ||||||
chr6:108633523
|
A | T | 1 | a0001c0001t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.622-29932A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633523 | ||||||
chr6:108633813
|
T | C | 1 | a0001c0001t0003g0273 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.622-29642T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633813 | ||||||
chr6:108633825
|
C | T | 3 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141 | 3 | HG02135.hp2 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.622-29630C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633825 | ||||||
chr6:108633842
|
T | TA | 23 | a0001c0001t0003g0037a0001c0001t0003g0134a0001c0001t0003g0135others(20): Show | 23 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.622-29599dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108633842 | |||||
chr6:108633842
|
TA | T | 20 | a0001c0001t0001g0034a0001c0001t0002g0208a0001c0001t0004g0001others(17): Show | 20 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.622-29599delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108633842 | |||||
chr6:108633938
|
T | C | 1 | a0001c0001t0015g0217 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.622-29517T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633938 | ||||||
chr6:108633996
|
C | A | 3 | a0002c0004t0001g0012a0002c0004t0001g0013a0002c0004t0001g0014 | 3 | HG00735.hp2 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.622-29459C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108633996 | ||||||
chr6:108634180
|
G | A | 15 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.622-29275G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108634180 | ||||||
chr6:108634334
|
C | T | 3 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141 | 3 | HG02135.hp2 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.622-29121C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108634334 | ||||||
chr6:108634434
|
G | A | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.622-29021G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108634434 | ||||||
chr6:108634538
|
G | A | 2 | a0001c0002t0002g0186a0001c0002t0003g0167 | 2 | NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.622-28917G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108634538 | ||||||
chr6:108634658
|
T | C | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-28797T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108634658 | ||||||
chr6:108635082
|
C | T | 1 | a0001c0001t0006g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.622-28373C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635082 | ||||||
chr6:108635113
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.622-28342C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635113 | ||||||
chr6:108635243
|
G | C | 15 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.622-28212G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635243 | ||||||
chr6:108635280
|
G | T | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.622-28175G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635280 | ||||||
chr6:108635301
|
A | T | 277 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.622-28154A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635301 | ||||||
chr6:108635585
|
T | C | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.622-27870T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635585 | ||||||
chr6:108635691
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-27764G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635691 | ||||||
chr6:108635830
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622-27625A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108635830 | ||||||
chr6:108636023
|
G | A | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.622-27432G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636023 | ||||||
chr6:108636047
|
C | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-27408C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636047 | ||||||
chr6:108636194
|
GC | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0114 | 3 | HG00639.hp2 HG01081.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622-27258delC | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108636194 | |||||
chr6:108636229
|
G | A | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-27226G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636229 | ||||||
chr6:108636229
|
G | C | 2 | a0001c0001t0005g0139a0001c0001t0005g0141 | 2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.622-27226G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636229 | ||||||
chr6:108636327
|
T | C | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-27128T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636327 | ||||||
chr6:108636374
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.622-27081C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636374 | ||||||
chr6:108636461
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.622-26994G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636461 | ||||||
chr6:108636493
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-26962G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636493 | ||||||
chr6:108636493
|
G | T | 1 | a0001c0001t0003g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.622-26962G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636493 | ||||||
chr6:108636503
|
T | A | 1 | a0001c0001t0003g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.622-26952T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636503 | ||||||
chr6:108636587
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-26868C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636587 | ||||||
chr6:108636668
|
G | A | 1 | a0001c0002t0002g0228 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.622-26787G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636668 | ||||||
chr6:108636904
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.622-26551G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108636904 | ||||||
chr6:108637143
|
G | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-26312G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637143 | ||||||
chr6:108637200
|
G | A | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-26255G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637200 | ||||||
chr6:108637441
|
A | C | 7 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-26014A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637441 | ||||||
chr6:108637693
|
T | C | 1 | a0001c0001t0003g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.622-25762T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637693 | ||||||
chr6:108637731
|
C | G | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-25724C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637731 | ||||||
chr6:108637792
|
T | C | 1 | a0001c0002t0002g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.622-25663T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637792 | ||||||
chr6:108637922
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.622-25533A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637922 | ||||||
chr6:108637977
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.622-25478T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637977 | ||||||
chr6:108637987
|
A | G | 2 | a0001c0001t0003g0151a0001c0001t0003g0200 | 2 | NA18954.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.622-25468A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637987 | ||||||
chr6:108637998
|
A | C | 1 | a0001c0001t0008g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.622-25457A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108637998 | ||||||
chr6:108638077
|
G | C | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-25378G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108638077 | ||||||
chr6:108638299
|
T | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-25156T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108638299 | ||||||
chr6:108638707
|
T | G | 16 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-24748T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108638707 | ||||||
chr6:108638822
|
T | G | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-24633T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108638822 | ||||||
chr6:108638889
|
A | G | 4 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0004others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-24566A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108638889 | ||||||
chr6:108639003
|
C | T | 1 | a0001c0002t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.622-24452C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639003 | ||||||
chr6:108639018
|
T | A | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-24437T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639018 | ||||||
chr6:108639383
|
T | G | 1 | a0001c0002t0035g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.622-24072T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639383 | ||||||
chr6:108639637
|
C | G | 69 | a0001c0001t0001g0033a0001c0001t0002g0035a0001c0001t0002g0208others(66): Show | 69 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.622-23818C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639637 | ||||||
chr6:108639654
|
T | C | 16 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-23801T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639654 | ||||||
chr6:108639800
|
C | T | 277 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.622-23655C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639800 | ||||||
chr6:108639905
|
A | G | 14 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.622-23550A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108639905 | ||||||
chr6:108640029
|
C | G | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-23426C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640029 | ||||||
chr6:108640100
|
C | T | 20 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.622-23355C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640100 | ||||||
chr6:108640139
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.622-23316G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640139 | ||||||
chr6:108640323
|
C | T | 14 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.622-23132C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640323 | ||||||
chr6:108640405
|
A | G | 2 | a0001c0001t0003g0016a0001c0001t0014g0047 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.622-23050A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640405 | ||||||
chr6:108640815
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-22640T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108640815 | ||||||
chr6:108641123
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-22332T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108641123 | ||||||
chr6:108641189
|
C | T | 1 | a0001c0001t0026g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.622-22266C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108641189 | ||||||
chr6:108641439
|
C | T | 68 | a0001c0001t0002g0035a0001c0001t0002g0208a0001c0001t0002g0242others(65): Show | 68 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.622-22016C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108641439 | ||||||
chr6:108641582
|
C | G | 2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.622-21873C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108641582 | ||||||
chr6:108641800
|
G | GA | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-21648dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108641800 | |||||
chr6:108642089
|
G | GT | 16 | a0001c0001t0001g0060a0001c0001t0004g0001a0001c0001t0004g0002others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-21349dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108642089 | |||||
chr6:108642089
|
G | GTT | 108 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.622-21350_622-2134 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108642089 | |||||
chr6:108642242
|
T | C | 16 | a0001c0001t0003g0017a0001c0001t0004g0001a0001c0001t0004g0002others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-21213T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108642242 | ||||||
chr6:108642344
|
A | G | 272 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.622-21111A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108642344 | ||||||
chr6:108642685
|
C | A | 3 | a0001c0001t0002g0208a0001c0001t0010g0174a0001c0001t0010g0189 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.622-20770C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108642685 | ||||||
chr6:108643022
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.622-20433C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643022 | ||||||
chr6:108643118
|
T | G | 1 | a0001c0001t0018g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.622-20337T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643118 | ||||||
chr6:108643312
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0244 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.622-20143G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643312 | ||||||
chr6:108643325
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.622-20130A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643325 | ||||||
chr6:108643404
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.622-20051A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643404 | ||||||
chr6:108643416
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.622-20039C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643416 | ||||||
chr6:108643682
|
A | G | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-19773A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643682 | ||||||
chr6:108643703
|
A | G | 4 | a0001c0001t0006g0247a0001c0001t0006g0248a0001c0001t0006g0250others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-19752A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643703 | ||||||
chr6:108643836
|
G | A | 101 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.622-19619G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643836 | ||||||
chr6:108643991
|
C | T | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.622-19464C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643991 | ||||||
chr6:108643996
|
T | C | 1 | a0001c0001t0027g0261 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.622-19459T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108643996 | ||||||
chr6:108644120
|
TCCCTCTC others(5): Show |
T | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-19329_622-1931 others(16): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108644120 | |||||
chr6:108644143
|
G | A | 1 | a0001c0001t0023g0119 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.622-19312G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644143 | ||||||
chr6:108644278
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-19177C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644278 | ||||||
chr6:108644293
|
C | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-19162C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644293 | ||||||
chr6:108644360
|
T | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-19095T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644360 | ||||||
chr6:108644790
|
G | T | 1 | a0001c0001t0045g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.622-18665G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644790 | ||||||
chr6:108644910
|
C | T | 14 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.622-18545C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108644910 | ||||||
chr6:108645066
|
C | T | 2 | a0001c0001t0003g0215a0001c0001t0003g0227 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622-18389C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108645066 | ||||||
chr6:108645458
|
C | CTT | 16 | a0001c0001t0003g0017a0001c0001t0005g0124a0001c0001t0005g0127others(13): Show | 16 | HG02145.hp1 HG02165.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-17983_622-1798 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108645458 | |||||
chr6:108645458
|
CT | C | 27 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(24): Show | 27 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.622-17982delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108645458 | |||||
chr6:108645458
|
CTT | C | 10 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-17983_622-1798 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108645458 | |||||
chr6:108645597
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-17858A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108645597 | ||||||
chr6:108645754
|
T | G | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-17701T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108645754 | ||||||
chr6:108646020
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-17435A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646020 | ||||||
chr6:108646131
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.622-17324G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646131 | ||||||
chr6:108646227
|
C | T | 1 | a0001c0001t0003g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.622-17228C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646227 | ||||||
chr6:108646479
|
T | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-16976T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646479 | ||||||
chr6:108646643
|
T | C | 275 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.622-16812T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646643 | ||||||
chr6:108646720
|
G | A | 2 | a0001c0001t0011g0147a0001c0001t0011g0148 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.622-16735G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646720 | ||||||
chr6:108646988
|
C | A | 14 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.622-16467C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108646988 | ||||||
chr6:108647228
|
T | G | 14 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.622-16227T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647228 | ||||||
chr6:108647237
|
G | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-16218G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647237 | ||||||
chr6:108647290
|
A | G | 2 | a0002c0004t0001g0013a0002c0004t0001g0014 | 2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.622-16165A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647290 | ||||||
chr6:108647474
|
G | C | 37 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-15981G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647474 | ||||||
chr6:108647596
|
A | C | 3 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0028g0277 | 3 | HG02698.hp1 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.622-15859A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647596 | ||||||
chr6:108647691
|
C | A | 2 | a0001c0001t0003g0203a0001c0001t0003g0207 | 2 | NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.622-15764C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647691 | ||||||
chr6:108647856
|
T | C | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0059others(4): Show | 7 | HG02074.hp2 NA18955.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-15599T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108647856 | ||||||
chr6:108648066
|
G | A | 1 | a0001c0002t0013g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.622-15389G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648066 | ||||||
chr6:108648132
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.622-15323C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648132 | ||||||
chr6:108648162
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.622-15293C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648162 | ||||||
chr6:108648267
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.622-15188G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648267 | ||||||
chr6:108648330
|
G | C | 1 | a0001c0001t0044g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.622-15125G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648330 | ||||||
chr6:108648383
|
T | C | 15 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.622-15072T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648383 | ||||||
chr6:108648413
|
C | T | 13 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.622-15042C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648413 | ||||||
chr6:108648525
|
C | T | 2 | a0001c0001t0003g0203a0001c0001t0003g0207 | 2 | NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.622-14930C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648525 | ||||||
chr6:108648548
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-14907T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648548 | ||||||
chr6:108648787
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0040 | 2 | NA18956.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.622-14668G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648787 | ||||||
chr6:108648841
|
T | A | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-14614T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648841 | ||||||
chr6:108648866
|
G | A | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-14589G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648866 | ||||||
chr6:108648902
|
T | A | 1 | a0001c0002t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.622-14553T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108648902 | ||||||
chr6:108649008
|
T | TA | 9 | a0001c0001t0002g0244a0001c0001t0003g0207a0001c0001t0004g0001others(6): Show | 9 | HG00140.hp2 HG01433.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-14422dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649008 | |||||
chr6:108649008
|
TA | T | 143 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.622-14422delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649008 | |||||
chr6:108649008
|
TAA | T | 8 | a0001c0001t0001g0073a0001c0001t0001g0094a0001c0001t0008g0122others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-14423_622-1442 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649008 | |||||
chr6:108649024
|
A | T | 10 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(7): Show | 10 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-14431A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649024 | ||||||
chr6:108649029
|
A | T | 10 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(7): Show | 10 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-14426A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649029 | ||||||
chr6:108649143
|
A | C | 1 | a0001c0001t0002g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.622-14312A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649143 | ||||||
chr6:108649160
|
C | A | 1 | a0001c0001t0017g0107 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.622-14295C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649160 | ||||||
chr6:108649181
|
G | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-14274G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649181 | ||||||
chr6:108649191
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-14264G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649191 | ||||||
chr6:108649195
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.622-14260G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649195 | ||||||
chr6:108649388
|
C | T | 2 | a0001c0001t0015g0201a0001c0001t0015g0217 | 2 | HG00673.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.622-14067C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649388 | ||||||
chr6:108649477
|
A | G | 38 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.622-13978A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649477 | ||||||
chr6:108649515
|
C | CT | 71 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0065others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.622-13914dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649515 | |||||
chr6:108649515
|
C | CTT | 11 | a0001c0001t0001g0026a0001c0001t0003g0017a0001c0001t0003g0155others(8): Show | 11 | HG02080.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-13915_622-1391 others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649515 | |||||
chr6:108649515
|
CT | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0002g0244others(6): Show | 9 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-13914delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108649515 | |||||
chr6:108649857
|
G | T | 20 | a0001c0001t0001g0023a0001c0001t0001g0058a0001c0001t0001g0060others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.622-13598G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108649857 | ||||||
chr6:108650010
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0099 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.622-13445A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650010 | ||||||
chr6:108650121
|
A | C | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13334A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650121 | ||||||
chr6:108650122
|
G | T | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13333G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650122 | ||||||
chr6:108650123
|
G | A | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13332G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650123 | ||||||
chr6:108650125
|
C | A | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13330C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650125 | ||||||
chr6:108650127
|
G | C | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13328G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650127 | ||||||
chr6:108650128
|
A | G | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13327A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650128 | ||||||
chr6:108650130
|
C | G | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13325C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650130 | ||||||
chr6:108650131
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13324C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650131 | ||||||
chr6:108650132
|
T | G | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13323T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650132 | ||||||
chr6:108650133
|
G | T | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13322G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650133 | ||||||
chr6:108650134
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.622-13321C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650134 | ||||||
chr6:108650163
|
A | G | 1 | a0001c0001t0007g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.622-13292A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650163 | ||||||
chr6:108650164
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0085 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.622-13291T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650164 | ||||||
chr6:108650187
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.622-13268C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650187 | ||||||
chr6:108650331
|
C | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-13124C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650331 | ||||||
chr6:108650370
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-13085G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650370 | ||||||
chr6:108650411
|
A | G | 3 | a0001c0001t0003g0221a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG02027.hp2 HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.622-13044A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650411 | ||||||
chr6:108650453
|
G | C | 38 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.622-13002G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650453 | ||||||
chr6:108650837
|
G | A | 1 | a0001c0001t0003g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.622-12618G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108650837 | ||||||
chr6:108651186
|
A | G | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-12269A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651186 | ||||||
chr6:108651326
|
A | C | 1 | a0001c0001t0003g0216 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.622-12129A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651326 | ||||||
chr6:108651331
|
A | C | 1 | a0001c0001t0044g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.622-12124A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651331 | ||||||
chr6:108651484
|
A | G | 4 | a0001c0002t0002g0149a0001c0002t0002g0168a0001c0002t0002g0169others(1): Show | 4 | NA18953.hp2 NA18966.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-11971A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651484 | ||||||
chr6:108651499
|
C | T | 20 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.622-11956C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651499 | ||||||
chr6:108651526
|
C | T | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-11929C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651526 | ||||||
chr6:108651621
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-11834G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651621 | ||||||
chr6:108651879
|
G | A | 1 | a0001c0002t0002g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.622-11576G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108651879 | ||||||
chr6:108652195
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622-11260G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652195 | ||||||
chr6:108652336
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.622-11119A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652336 | ||||||
chr6:108652699
|
C | T | 20 | a0001c0001t0003g0037a0001c0001t0003g0155a0001c0001t0003g0262others(17): Show | 20 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.622-10756C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652699 | ||||||
chr6:108652756
|
A | G | 1 | a0001c0001t0003g0266 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.622-10699A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652756 | ||||||
chr6:108652895
|
C | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.622-10560C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652895 | ||||||
chr6:108652964
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.622-10491C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108652964 | ||||||
chr6:108653250
|
C | A | 38 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.622-10205C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653250 | ||||||
chr6:108653375
|
C | G | 38 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.622-10080C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653375 | ||||||
chr6:108653530
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.622-9925C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653530 | ||||||
chr6:108653543
|
A | C | 112 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.622-9912A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653543 | ||||||
chr6:108653674
|
T | C | 17 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.622-9781T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653674 | ||||||
chr6:108653750
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-9705A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108653750 | ||||||
chr6:108654035
|
A | G | 3 | a0001c0001t0001g0105a0001c0001t0008g0095a0001c0001t0042g0043 | 3 | HG01255.hp2 HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.622-9420A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654035 | ||||||
chr6:108654151
|
G | T | 1 | a0001c0002t0002g0149 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.622-9304G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654151 | ||||||
chr6:108654157
|
A | C | 1 | a0001c0002t0002g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.622-9298A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654157 | ||||||
chr6:108654261
|
C | G | 53 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(50): Show | 53 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.622-9194C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654261 | ||||||
chr6:108654301
|
GAAA | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-9150_622-9148d others(5): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108654301 | |||||
chr6:108654359
|
C | T | 53 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(50): Show | 53 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.622-9096C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654359 | ||||||
chr6:108654393
|
T | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0021g0015 | 3 | HG03098.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.622-9062T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654393 | ||||||
chr6:108654443
|
G | A | 69 | a0001c0001t0002g0035a0001c0001t0002g0208a0001c0001t0002g0242others(66): Show | 69 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.622-9012G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654443 | ||||||
chr6:108654495
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-8960G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654495 | ||||||
chr6:108654592
|
CT | C | 4 | a0001c0001t0002g0208a0001c0002t0002g0190a0001c0002t0002g0193others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-8862delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654592 | ||||||
chr6:108654610
|
G | C | 1 | a0001c0001t0003g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.622-8845G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654610 | ||||||
chr6:108654629
|
C | T | 1 | a0001c0003t0016g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.622-8826C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654629 | ||||||
chr6:108654737
|
C | CT | 10 | a0001c0001t0001g0045a0001c0001t0004g0001a0001c0001t0004g0002others(7): Show | 10 | HG01243.hp1 HG01981.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-8703dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108654737 | |||||
chr6:108654737
|
CT | C | 9 | a0001c0001t0001g0096a0001c0001t0012g0173a0001c0001t0012g0199others(6): Show | 9 | HG00323.hp2 HG01256.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-8703delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108654737 | |||||
chr6:108654754
|
A | C | 1 | a0001c0001t0007g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.622-8701A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654754 | ||||||
chr6:108654952
|
A | G | 9 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(6): Show | 9 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-8503A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654952 | ||||||
chr6:108654988
|
C | T | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-8467C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108654988 | ||||||
chr6:108655114
|
G | A | 1 | a0001c0001t0020g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.622-8341G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655114 | ||||||
chr6:108655208
|
G | C | 1 | a0001c0001t0004g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.622-8247G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655208 | ||||||
chr6:108655382
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.622-8073T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655382 | ||||||
chr6:108655409
|
T | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0021g0015 | 3 | HG03098.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.622-8046T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655409 | ||||||
chr6:108655499
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.622-7956G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655499 | ||||||
chr6:108655904
|
A | G | 53 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(50): Show | 53 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.622-7551A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655904 | ||||||
chr6:108655944
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.622-7511C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108655944 | ||||||
chr6:108656040
|
G | A | 1 | a0001c0001t0003g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.622-7415G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656040 | ||||||
chr6:108656135
|
C | CA | 20 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(17): Show | 20 | HG00280.hp2 HG00639.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.622-7309dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108656135 | |||||
chr6:108656135
|
C | CAA | 18 | a0001c0001t0003g0151a0001c0001t0003g0153a0001c0001t0003g0196others(15): Show | 18 | HG00438.hp2 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.622-7310_622-7309d others(4): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 108656135 | |||||
chr6:108656145
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.622-7310A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656145 | ||||||
chr6:108656351
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.622-7104G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656351 | ||||||
chr6:108656460
|
T | C | 111 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.622-6995T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656460 | ||||||
chr6:108656494
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-6961C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656494 | ||||||
chr6:108656531
|
G | A | 1 | a0001c0001t0014g0267 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.622-6924G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656531 | ||||||
chr6:108656551
|
T | A | 8 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-6904T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108656551 | ||||||
chr6:108657571
|
A | G | 13 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.622-5884A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108657571 | ||||||
chr6:108657978
|
C | G | 3 | a0001c0001t0017g0071a0001c0001t0017g0107a0001c0001t0031g0068 | 3 | HG00673.hp2 HG02132.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.622-5477C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108657978 | ||||||
chr6:108658023
|
C | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-5432C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658023 | ||||||
chr6:108658059
|
T | G | 1 | a0001c0001t0020g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.622-5396T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658059 | ||||||
chr6:108658103
|
C | T | 7 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0194others(4): Show | 7 | HG00140.hp2 HG01123.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-5352C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658103 | ||||||
chr6:108658411
|
A | C | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-5044A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658411 | ||||||
chr6:108658663
|
T | C | 1 | a0001c0001t0041g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-4792T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658663 | ||||||
chr6:108658672
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-4783G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658672 | ||||||
chr6:108658692
|
A | G | 13 | a0001c0001t0003g0016a0001c0001t0004g0001a0001c0001t0004g0002others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.622-4763A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658692 | ||||||
chr6:108658743
|
T | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-4712T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658743 | ||||||
chr6:108658884
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4571T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658884 | ||||||
chr6:108658885
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4570T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658885 | ||||||
chr6:108658886
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4569T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658886 | ||||||
chr6:108658888
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4567G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658888 | ||||||
chr6:108658889
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4566T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658889 | ||||||
chr6:108658891
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4564T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658891 | ||||||
chr6:108658892
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4563G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658892 | ||||||
chr6:108658894
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4561T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658894 | ||||||
chr6:108658896
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-4559G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658896 | ||||||
chr6:108658913
|
T | C | 12 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.622-4542T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658913 | ||||||
chr6:108658977
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.622-4478C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108658977 | ||||||
chr6:108659090
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.622-4365G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659090 | ||||||
chr6:108659215
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0092 | 2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.622-4240A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659215 | ||||||
chr6:108659300
|
T | C | 1 | a0001c0001t0011g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.622-4155T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659300 | ||||||
chr6:108659315
|
G | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-4140G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659315 | ||||||
chr6:108659827
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622-3628C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659827 | ||||||
chr6:108659878
|
A | G | 1 | a0001c0002t0002g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.622-3577A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659878 | ||||||
chr6:108659914
|
A | G | 248 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.622-3541A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659914 | ||||||
chr6:108659946
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.622-3509C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659946 | ||||||
chr6:108659954
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.622-3501C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659954 | ||||||
chr6:108659993
|
T | G | 51 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.622-3462T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108659993 | ||||||
chr6:108660135
|
G | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-3320G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660135 | ||||||
chr6:108660217
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.622-3238G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660217 | ||||||
chr6:108660222
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.622-3233C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660222 | ||||||
chr6:108660345
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.622-3110A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660345 | ||||||
chr6:108660347
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0008g0084 | 2 | NA18953.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.622-3108C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660347 | ||||||
chr6:108660357
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-3098A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660357 | ||||||
chr6:108660372
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3083C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660372 | ||||||
chr6:108660374
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3081C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660374 | ||||||
chr6:108660376
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3079T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660376 | ||||||
chr6:108660377
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3078G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660377 | ||||||
chr6:108660378
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3077G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660378 | ||||||
chr6:108660380
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3075C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660380 | ||||||
chr6:108660381
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3074A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660381 | ||||||
chr6:108660384
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3071A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660384 | ||||||
chr6:108660385
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.622-3070T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660385 | ||||||
chr6:108660399
|
T | C | 1 | a0001c0001t0003g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.622-3056T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660399 | ||||||
chr6:108660564
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.622-2891C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660564 | ||||||
chr6:108660726
|
G | T | 1 | a0001c0001t0006g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.622-2729G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660726 | ||||||
chr6:108660758
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.622-2697G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108660758 | ||||||
chr6:108661032
|
C | T | 2 | a0001c0001t0003g0205a0001c0001t0003g0206 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.622-2423C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661032 | ||||||
chr6:108661079
|
C | T | 39 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(36): Show | 39 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.622-2376C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661079 | ||||||
chr6:108661113
|
G | T | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-2342G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661113 | ||||||
chr6:108661114
|
C | T | 1 | a0001c0001t0045g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.622-2341C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661114 | ||||||
chr6:108661206
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622-2249C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661206 | ||||||
chr6:108661256
|
A | G | 11 | a0001c0002t0002g0156a0001c0002t0002g0160a0001c0002t0002g0161others(8): Show | 11 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-2199A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661256 | ||||||
chr6:108661306
|
G | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-2149G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661306 | ||||||
chr6:108661336
|
G | A | 23 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(20): Show | 23 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.622-2119G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661336 | ||||||
chr6:108661389
|
G | GC | 248 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.622-2066_622-2065i others(3): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661389 | ||||||
chr6:108661521
|
G | A | 1 | a0001c0002t0002g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.622-1934G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661521 | ||||||
chr6:108661544
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.622-1911A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661544 | ||||||
chr6:108661670
|
A | G | 3 | a0001c0001t0006g0247a0001c0001t0006g0248a0001c0001t0034g0246 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.622-1785A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661670 | ||||||
chr6:108661678
|
T | C | 9 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(6): Show | 9 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-1777T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661678 | ||||||
chr6:108661906
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-1549T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661906 | ||||||
chr6:108661959
|
T | C | 2 | a0001c0001t0003g0150a0001c0001t0003g0226 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.622-1496T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108661959 | ||||||
chr6:108662112
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.622-1343A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662112 | ||||||
chr6:108662171
|
G | A | 4 | a0001c0002t0002g0149a0001c0002t0002g0168a0001c0002t0002g0169others(1): Show | 4 | NA18953.hp2 NA18966.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-1284G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662171 | ||||||
chr6:108662256
|
G | A | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.622-1199G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662256 | ||||||
chr6:108662288
|
A | C | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.622-1167A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662288 | ||||||
chr6:108662324
|
C | T | 110 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.622-1131C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662324 | ||||||
chr6:108662503
|
T | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-952T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662503 | ||||||
chr6:108662657
|
C | T | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.622-798C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662657 | ||||||
chr6:108662864
|
A | G | 39 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(36): Show | 39 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.622-591A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662864 | ||||||
chr6:108662904
|
A | G | 1 | a0001c0001t0014g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.622-551A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108662904 | ||||||
chr6:108663004
|
A | G | 2 | a0001c0002t0002g0230a0001c0002t0002g0231 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.622-451A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663004 | ||||||
chr6:108663049
|
T | C | 2 | a0001c0001t0003g0215a0001c0001t0003g0227 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622-406T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663049 | ||||||
chr6:108663087
|
G | A | 1 | a0001c0001t0009g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.622-368G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663087 | ||||||
chr6:108663243
|
G | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.622-212G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663243 | ||||||
chr6:108663277
|
C | T | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.622-178C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663277 | ||||||
chr6:108663392
|
C | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-63C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108663392 | ||||||
chr6:108665080
|
C | T | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*34+191C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108665080 | ||||||
chr6:108665403
|
G | A | 52 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(49): Show | 52 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.*34+514G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108665403 | ||||||
chr6:108665470
|
T | C | 1 | a0001c0002t0002g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*34+581T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108665470 | ||||||
chr6:108665764
|
G | A | 1 | a0001c0001t0003g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.*34+875G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108665764 | ||||||
chr6:108665812
|
G | GA | 107 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.*34+940dupA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108665812 | |||||
chr6:108665812
|
GA | G | 99 | a0001c0001t0002g0035a0001c0001t0002g0130a0001c0001t0002g0131others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.*34+940delA | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108665812 | |||||
chr6:108665948
|
G | A | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*34+1059G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108665948 | ||||||
chr6:108666024
|
T | TGTG | 52 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(49): Show | 52 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.*34+1137_*34+1138i others(5): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108666024 | |||||
chr6:108666044
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*34+1155T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666044 | ||||||
chr6:108666115
|
T | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.*34+1226T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666115 | ||||||
chr6:108666337
|
T | C | 1 | a0001c0002t0002g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*34+1448T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666337 | ||||||
chr6:108666343
|
TC | T | 10 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.*34+1455delC | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666343 | ||||||
chr6:108666391
|
A | G | 1 | a0001c0001t0003g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*34+1502A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666391 | ||||||
chr6:108666416
|
A | G | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.*34+1527A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666416 | ||||||
chr6:108666473
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*34+1584C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666473 | ||||||
chr6:108666517
|
T | A | 2 | a0001c0001t0005g0137a0001c0002t0002g0177 | 2 | HG03579.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.*34+1628T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666517 | ||||||
chr6:108666564
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*34+1675C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666564 | ||||||
chr6:108666754
|
G | GT | 11 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.*34+1866dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108666754 | |||||
chr6:108666787
|
T | C | 1 | a0001c0002t0002g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*34+1898T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666787 | ||||||
chr6:108666981
|
G | A | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.*34+2092G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108666981 | ||||||
chr6:108667392
|
T | C | 38 | a0001c0001t0002g0152a0001c0001t0003g0150a0001c0001t0003g0151others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.*34+2503T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108667392 | ||||||
chr6:108667517
|
C | G | 2 | a0001c0001t0003g0016a0001c0001t0014g0047 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.*34+2628C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108667517 | ||||||
chr6:108667890
|
A | G | 1 | a0001c0001t0034g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*34+3001A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108667890 | ||||||
chr6:108668355
|
A | T | 1 | a0001c0001t0014g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*34+3466A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668355 | ||||||
chr6:108668460
|
T | C | 2 | a0001c0001t0011g0145a0001c0001t0011g0146 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.*34+3571T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668460 | ||||||
chr6:108668702
|
C | G | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.*34+3813C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668702 | ||||||
chr6:108668749
|
A | T | 4 | a0001c0001t0003g0204a0001c0001t0003g0221a0001c0001t0003g0237others(1): Show | 4 | HG00438.hp2 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.*34+3860A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668749 | ||||||
chr6:108668750
|
C | A | 4 | a0001c0001t0003g0204a0001c0001t0003g0221a0001c0001t0003g0237others(1): Show | 4 | HG00438.hp2 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.*34+3861C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668750 | ||||||
chr6:108668751
|
TC | T | 4 | a0001c0001t0003g0204a0001c0001t0003g0221a0001c0001t0003g0237others(1): Show | 4 | HG00438.hp2 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.*34+3863delC | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668751 | ||||||
chr6:108668904
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.*34+4015A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108668904 | ||||||
chr6:108669004
|
C | T | 5 | a0001c0001t0003g0195a0001c0001t0003g0197a0001c0001t0003g0205others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.*34+4115C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669004 | ||||||
chr6:108669019
|
A | G | 1 | a0001c0001t0021g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*34+4130A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669019 | ||||||
chr6:108669579
|
T | C | 12 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.*34+4690T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669579 | ||||||
chr6:108669602
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*34+4713C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669602 | ||||||
chr6:108669638
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.*34+4749G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669638 | ||||||
chr6:108669663
|
G | A | 4 | a0001c0002t0002g0209a0001c0002t0002g0210a0001c0002t0002g0211others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.*34+4774G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669663 | ||||||
chr6:108669729
|
G | A | 1 | a0001c0002t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*34+4840G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669729 | ||||||
chr6:108669749
|
A | G | 1 | a0001c0002t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.*34+4860A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669749 | ||||||
chr6:108669787
|
T | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0099 | 3 | HG01256.hp1 HG01258.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.*34+4898T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669787 | ||||||
chr6:108669835
|
C | T | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*34+4946C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669835 | ||||||
chr6:108669936
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*34+5047C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108669936 | ||||||
chr6:108670065
|
T | C | 274 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.*34+5176T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670065 | ||||||
chr6:108670267
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.*34+5378C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670267 | ||||||
chr6:108670483
|
G | T | 39 | a0001c0001t0002g0152a0001c0001t0003g0017a0001c0001t0003g0150others(36): Show | 39 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.*34+5594G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670483 | ||||||
chr6:108670583
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*34+5694G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670583 | ||||||
chr6:108670603
|
T | C | 257 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.*34+5714T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670603 | ||||||
chr6:108670646
|
T | G | 1 | a0001c0002t0002g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*34+5757T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108670646 | ||||||
chr6:108671001
|
C | T | 1 | a0001c0002t0002g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*34+6112C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671001 | ||||||
chr6:108671139
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.*34+6250A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671139 | ||||||
chr6:108671443
|
G | A | 13 | a0001c0001t0003g0155a0001c0001t0003g0262a0001c0001t0003g0263others(10): Show | 13 | HG00323.hp2 HG02071.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.*34+6554G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671443 | ||||||
chr6:108671482
|
G | A | 12 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(9): Show | 12 | HG02135.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.*34+6593G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671482 | ||||||
chr6:108671608
|
A | G | 277 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.*34+6719A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671608 | ||||||
chr6:108671693
|
C | T | 1 | a0001c0002t0019g0179 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.*34+6804C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108671693 | ||||||
chr6:108672196
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.*34+7307G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672196 | ||||||
chr6:108672247
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.*34+7358G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672247 | ||||||
chr6:108672320
|
A | G | 3 | a0001c0001t0020g0018a0001c0001t0020g0019a0001c0001t0021g0015 | 3 | HG02976.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.*34+7431A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672320 | ||||||
chr6:108672337
|
C | G | 1 | a0001c0001t0008g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.*34+7448C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672337 | ||||||
chr6:108672469
|
A | G | 1 | a0001c0002t0002g0166 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.*35-7358A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672469 | ||||||
chr6:108672486
|
TTG | T | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0002t0013g0234 | 3 | HG02818.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.*35-7337_*35-7336d others(4): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108672486 | |||||
chr6:108672844
|
AT | A | 7 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG02922.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.*35-6976delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108672844 | |||||
chr6:108672958
|
A | G | 111 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.*35-6869A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672958 | ||||||
chr6:108672969
|
G | A | 1 | a0001c0001t0014g0267 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*35-6858G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108672969 | ||||||
chr6:108673102
|
A | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*35-6725A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673102 | ||||||
chr6:108673230
|
C | T | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.*35-6597C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673230 | ||||||
chr6:108673356
|
C | A | 1 | a0001c0002t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*35-6471C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673356 | ||||||
chr6:108673623
|
G | A | 100 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.*35-6204G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673623 | ||||||
chr6:108673666
|
G | A | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*35-6161G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673666 | ||||||
chr6:108673757
|
G | A | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*35-6070G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673757 | ||||||
chr6:108673766
|
A | G | 8 | a0001c0001t0007g0028a0001c0001t0007g0029a0001c0001t0007g0030others(5): Show | 8 | HG01081.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.*35-6061A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673766 | ||||||
chr6:108673984
|
A | G | 63 | a0001c0001t0002g0152a0001c0001t0003g0016a0001c0001t0003g0017others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.*35-5843A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108673984 | ||||||
chr6:108674060
|
C | T | 2 | a0001c0001t0003g0215a0001c0001t0003g0227 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.*35-5767C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674060 | ||||||
chr6:108674212
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0098others(1): Show | 4 | HG01106.hp1 HG01123.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35-5615T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674212 | ||||||
chr6:108674463
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.*35-5364G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674463 | ||||||
chr6:108674503
|
T | C | 3 | a0001c0001t0012g0173a0001c0001t0012g0199a0001c0001t0012g0202 | 3 | NA18968.hp1 NA19010.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.*35-5324T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674503 | ||||||
chr6:108674771
|
C | T | 2 | a0001c0001t0021g0015a0001c0001t0040g0032 | 2 | HG01106.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.*35-5056C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674771 | ||||||
chr6:108674978
|
T | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0114 | 3 | HG00639.hp2 HG01081.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.*35-4849T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108674978 | ||||||
chr6:108675120
|
C | A | 1 | a0001c0001t0014g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*35-4707C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675120 | ||||||
chr6:108675185
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*35-4642C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675185 | ||||||
chr6:108675212
|
G | T | 9 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0245others(6): Show | 9 | HG02055.hp2 HG02165.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.*35-4615G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675212 | ||||||
chr6:108675350
|
T | C | 179 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.*35-4477T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675350 | ||||||
chr6:108675374
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*35-4453G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675374 | ||||||
chr6:108675436
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*35-4391G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675436 | ||||||
chr6:108675444
|
A | G | 3 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0028g0277 | 3 | HG02698.hp1 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.*35-4383A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675444 | ||||||
chr6:108675545
|
T | G | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-4282T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675545 | ||||||
chr6:108675549
|
A | G | 1 | a0001c0001t0026g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.*35-4278A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675549 | ||||||
chr6:108675700
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*35-4127A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675700 | ||||||
chr6:108675760
|
G | T | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-4067G>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108675760 | ||||||
chr6:108676232
|
G | A | 101 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.*35-3595G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676232 | ||||||
chr6:108676237
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.*35-3590G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676237 | ||||||
chr6:108676393
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.*35-3434C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676393 | ||||||
chr6:108676408
|
G | A | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-3419G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676408 | ||||||
chr6:108676429
|
A | T | 1 | a0001c0001t0006g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*35-3398A>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676429 | ||||||
chr6:108676448
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.*35-3379C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676448 | ||||||
chr6:108676925
|
T | G | 63 | a0001c0001t0002g0152a0001c0001t0003g0016a0001c0001t0003g0017others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.*35-2902T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108676925 | ||||||
chr6:108677063
|
A | G | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-2764A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677063 | ||||||
chr6:108677180
|
T | G | 1 | a0001c0002t0002g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*35-2647T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677180 | ||||||
chr6:108677237
|
G | A | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*35-2590G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677237 | ||||||
chr6:108677499
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*35-2328G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677499 | ||||||
chr6:108677576
|
G | A | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*35-2251G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677576 | ||||||
chr6:108677702
|
G | C | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-2125G>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677702 | ||||||
chr6:108677747
|
T | G | 1 | a0001c0001t0013g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*35-2080T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677747 | ||||||
chr6:108677750
|
C | T | 63 | a0001c0001t0002g0152a0001c0001t0003g0016a0001c0001t0003g0017others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.*35-2077C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677750 | ||||||
chr6:108677860
|
C | A | 1 | a0001c0001t0008g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.*35-1967C>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677860 | ||||||
chr6:108677898
|
G | A | 101 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.*35-1929G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677898 | ||||||
chr6:108677983
|
A | G | 2 | a0001c0001t0003g0216a0001c0001t0024g0229 | 2 | NA18747.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.*35-1844A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677983 | ||||||
chr6:108677992
|
A | G | 269 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.*35-1835A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108677992 | ||||||
chr6:108678084
|
A | G | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-1743A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678084 | ||||||
chr6:108678493
|
C | CT | 99 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.*35-1318dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678493 | |||||
chr6:108678493
|
CT | C | 71 | a0001c0001t0002g0130a0001c0001t0002g0152a0001c0001t0003g0016others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.*35-1318delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678493 | |||||
chr6:108678710
|
T | G | 1 | a0001c0001t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*35-1117T>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678710 | ||||||
chr6:108678763
|
C | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35-1064C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678763 | ||||||
chr6:108678869
|
C | CTTTTTTT | 33 | a0001c0001t0003g0134a0001c0001t0003g0135a0001c0001t0003g0150others(30): Show | 33 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.*35-942_*35-936dup others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678869
|
C | CTTTTTTT others(1): Show |
25 | a0001c0001t0002g0152a0001c0001t0003g0016a0001c0001t0003g0017others(22): Show | 25 | HG00639.hp1 HG00673.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.*35-943_*35-936dup others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678869
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*35-945_*35-936dup others(10): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678869
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0003g0223 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*35-946_*35-936dup others(11): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678869
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0098others(1): Show | 4 | HG01106.hp1 HG01123.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35-958C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678869 | ||||||
chr6:108678869
|
CT | C | 21 | a0001c0001t0002g0243a0001c0001t0006g0010a0001c0001t0006g0245others(18): Show | 21 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.*35-936delT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678869
|
CTT | C | 5 | a0001c0001t0002g0242a0001c0001t0006g0011a0001c0001t0011g0147others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35-937_*35-936del others(2): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678869 | |||||
chr6:108678890
|
T | TTTTTTC | 5 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0072others(2): Show | 5 | HG03017.hp2 NA18945.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35-936_*35-935ins others(6): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678890 | |||||
chr6:108678890
|
T | TTTTTTTC | 76 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.*35-936_*35-935ins others(7): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678890 | |||||
chr6:108678890
|
T | TTTTTTTT others(1): Show |
16 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0055others(13): Show | 16 | HG00438.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.*35-936_*35-935ins others(8): Show |
FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108678890 | |||||
chr6:108678897
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*35-930G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678897 | ||||||
chr6:108678957
|
T | C | 1 | a0001c0001t0040g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*35-870T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678957 | ||||||
chr6:108678972
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*35-855C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108678972 | ||||||
chr6:108679020
|
C | G | 1 | a0001c0001t0045g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.*35-807C>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679020 | ||||||
chr6:108679073
|
A | G | 167 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.*35-754A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679073 | ||||||
chr6:108679076
|
T | A | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.*35-751T>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679076 | ||||||
chr6:108679078
|
A | G | 7 | a0001c0001t0003g0153a0001c0001t0003g0204a0001c0001t0003g0219others(4): Show | 7 | HG00438.hp2 HG02027.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.*35-749A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679078 | ||||||
chr6:108679113
|
T | C | 105 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.*35-714T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679113 | ||||||
chr6:108679128
|
T | C | 277 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.*35-699T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679128 | ||||||
chr6:108679162
|
C | T | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.*35-665C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679162 | ||||||
chr6:108679273
|
T | C | 2 | a0001c0001t0020g0018a0001c0001t0020g0019 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.*35-554T>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679273 | ||||||
chr6:108679297
|
A | AT | 63 | a0001c0001t0002g0152a0001c0001t0003g0016a0001c0001t0003g0017others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.*35-527dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108679297 | |||||
chr6:108679314
|
G | GT | 8 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0005g0137others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.*35-511dupT | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 108679314 | |||||
chr6:108679413
|
G | A | 1 | a0001c0002t0002g0228 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.*35-414G>A | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679413 | ||||||
chr6:108679415
|
C | T | 1 | a0001c0001t0022g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*35-412C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679415 | ||||||
chr6:108679519
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0008g0084 | 2 | NA18953.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.*35-308C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679519 | ||||||
chr6:108679539
|
A | G | 103 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.*35-288A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679539 | ||||||
chr6:108679613
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*35-214A>C | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 2/2 | chr6 | 108679613 |