Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MAEAP others(668): Show |
chr6 | 108555917 | 108689774 |
| a0002 | 0/0 | 673 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | MAEAP others(668): Show |
chr6 | 108555917 | 108689774 |
| a0003 | 0/0 | 673 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | MAEAP others(668): Show |
chr6 | 108555917 | 108689774 |
| a0004 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | MAEAP others(668): Show |
chr6 | 108555917 | 108689774 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2019 | 214 | 70 | 25 | 81 | 13 | 24 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0001c0002 | 0/1 | 2019 | 54 | 17 | 15 | 11 | 3 | 7 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0001c0003 | 0/0 | 2019 | 3 | 0 | 0 | 2 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0001c0006 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0001c0007 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0002c0004 | 0/0 | 2019 | 3 | 0 | 2 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0003c0008 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
chr6 | 108555917 | 108689774 | ||
| a0004c0005 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | ATGGC others(2014): Show |
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 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0002 | 0/0 | 7296 | 11 | 10 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0003 | 0/0 | 7297 | 47 | 9 | 1 | 28 | 3 | 6 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0004 | 0/0 | 7296 | 8 | 7 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0005 | 0/0 | 7293 | 7 | 6 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7288): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0006 | 0/0 | 7297 | 6 | 3 | 0 | 3 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0007 | 0/0 | 7296 | 6 | 5 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0008 | 0/0 | 7299 | 6 | 1 | 1 | 4 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7294): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0009 | 0/0 | 7293 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7288): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0010 | 0/0 | 7296 | 3 | 3 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0011 | 0/0 | 7296 | 4 | 4 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0012 | 0/0 | 7297 | 3 | 0 | 0 | 3 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0013 | 0/0 | 7296 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0014 | 0/0 | 7298 | 2 | 1 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0015 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0017 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0018 | 0/0 | 7298 | 2 | 0 | 1 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0020 | 0/0 | 7296 | 2 | 2 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0021 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0022 | 0/0 | 7293 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7288): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0023 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0024 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0025 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0026 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0027 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0028 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0029 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0030 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0031 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0032 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0033 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0034 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0037 | 1/0 | 7296 | 1 | 0 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0040 | 0/0 | 7296 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0041 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0042 | 0/0 | 7298 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0043 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0044 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0001t0045 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0001 | 0/0 | 7298 | 2 | 0 | 1 | 0 | 1 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0002 | 0/1 | 7296 | 42 | 14 | 12 | 8 | 2 | 5 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0003 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0010 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0013 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0019 | 0/0 | 7297 | 2 | 0 | 0 | 2 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0021 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0035 | 0/0 | 7297 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0036 | 0/0 | 7298 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0038 | 0/0 | 7296 | 1 | 0 | 1 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0002t0039 | 0/0 | 7296 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
chr6 | 108555917 | 108689774 |
| a0001c0003t0003 | 0/0 | 7297 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0003t0016 | 0/0 | 7297 | 2 | 0 | 0 | 1 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0001c0006t0001 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0001c0007t0006 | 0/0 | 7297 | 1 | 0 | 0 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7292): Show |
chr6 | 108555917 | 108689774 |
| a0002c0004t0001 | 0/0 | 7298 | 3 | 0 | 2 | 0 | 0 | 1 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0003c0008t0001 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7293): Show |
chr6 | 108555917 | 108689774 |
| a0004c0005t0007 | 0/0 | 7296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | GGTGT others(7291): Show |
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 |
| a0003c0008t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
| a0004c0005t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 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 | a0003 | 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 | a0004 | 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 | a0001 | c0002 | t0002 | g0212 | REF | REF | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0037 | g0126 | REF | REF | FOXO3_chr6_108555917_108689774 | FOXO3 | chr6 | 108555917 | 108689774 |
| view | 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 | a0003 | 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 | a0004 | 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 |
| view | 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 | 53 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(50): 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 |
| view | 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 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0022 |
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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(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 | a0001c0001t0008 a0001c0001t0014 |
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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0017 others(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 | a0001c0001t0007 a0004c0005t0007 |
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 | a0001c0001t0030 a0001c0002t0039 |
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 | a0001c0001t0004 a0001c0001t0033 |
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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0017 others(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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0017 others(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 | a0001c0001t0013 a0001c0002t0013 |
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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0018 others(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 | a0001c0001t0006 a0001c0001t0026 a0001c0001t0034 others(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 | a0001c0001t0010 a0001c0002t0010 |
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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(36): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*4593A>G | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 3/3 | 19530 | chr6 | 108684385 |
| view | 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 | a0001c0001t0001g0259 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0001g0259 a0001c0001t0002g0258 a0001c0001t0003g0262 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 |
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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0003c0008t0001g0256 | 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 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0001g0259 a0001c0001t0002g0258 a0001c0001t0003g0262 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0239 a0001c0001t0002g0242 a0001c0001t0002g0243 others(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 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
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 | 96 | a0001c0001t0002g0152 a0001c0001t0002g0208 a0001c0001t0002g0242 others(93): Show |
96 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(93): 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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0032g0143 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | 242 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): 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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 |
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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0002t0002g0236 a0001c0002t0002g0255 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0235 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0008g0122 a0001c0001t0018g0120 a0001c0001t0018g0121 others(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 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | 270 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(267): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0001g0259 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0151 others(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 | a0001c0001t0001g0034 a0001c0001t0002g0035 a0001c0001t0010g0036 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0005g0127 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0011g0145 a0001c0002t0002g0149 a0001c0002t0002g0158 others(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 | a0001c0001t0010g0174 a0001c0001t0011g0146 a0001c0001t0012g0173 others(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 | a0001c0001t0002g0242 a0001c0001t0010g0189 a0001c0001t0011g0147 others(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 | 22 | a0001c0001t0002g0208 a0001c0001t0003g0150 a0001c0001t0003g0151 others(19): Show |
22 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(19): 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 | a0001c0001t0002g0243 a0001c0001t0003g0214 a0001c0001t0003g0215 others(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 | a0001c0001t0003g0224 a0001c0001t0003g0226 a0001c0001t0003g0227 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0270 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0272 a0001c0001t0003g0273 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0001g0117 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | 53 | a0001c0002t0001g0178 a0001c0002t0001g0184 a0001c0002t0002g0149 others(50): Show |
53 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(50): 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 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0002g0156 a0001c0002t0002g0160 a0001c0002t0002g0161 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0002g0187 a0001c0002t0002g0188 |
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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0244 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | 266 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | 265 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.621+14890C>T | FOXO3 | ENSG00000118689.15 | transcript | ENST00000406360.2 | protein_coding | 1/2 | chr6 | 108576719 | |||||||
| chr6:108577202 | T | TA | 263 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
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 | a0001c0001t0002g0258 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0004c0005t0007g0031 | 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 | 222 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): 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 | a0001c0001t0001g0025 a0001c0001t0001g0106 a0001c0001t0001g0116 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | 53 | a0001c0002t0001g0178 a0001c0002t0001g0184 a0001c0002t0002g0149 others(50): Show |
53 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(50): 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 | a0001c0001t0006g0010 a0001c0001t0006g0011 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | 266 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0235 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0005 a0001c0001t0004g0008 others(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 | 265 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | 96 | a0001c0001t0002g0152 a0001c0001t0002g0208 a0001c0001t0002g0242 others(93): Show |
96 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(93): 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 | a0001c0001t0002g0131 a0001c0001t0002g0152 a0001c0001t0002g0208 others(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 | 30 | a0001c0001t0001g0034 a0001c0001t0003g0265 a0001c0001t0003g0268 others(27): Show |
30 | HG00140.hp2 HG01123.hp1 HG01192.hp1 others(27): 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 | a0001c0001t0001g0053 a0001c0001t0002g0035 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0102 others(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 | a0001c0001t0002g0208 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0226 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0006g0247 a0001c0001t0006g0248 a0001c0001t0006g0250 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0002t0002g0186 a0001c0002t0003g0167 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0001g0074 a0001c0001t0002g0132 a0001c0001t0003g0195 others(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 | a0001c0001t0003g0216 a0001c0001t0005g0124 a0001c0001t0005g0127 others(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 | 57 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(54): Show |
57 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(54): 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 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0003g0016 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0004 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0001g0252 |
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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0063 others(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 | a0001c0001t0002g0258 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0003g0016 a0001c0001t0014g0047 |
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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | a0001c0001t0002g0258 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 |
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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0003g0197 a0001c0001t0003g0205 a0001c0001t0003g0206 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | 144 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0093 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(141): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 a0002c0004t0001g0012 others(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 | a0001c0001t0001g0087 a0001c0001t0002g0130 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0093 a0001c0001t0001g0111 others(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 | 50 | a0001c0001t0001g0033 a0001c0001t0002g0242 a0001c0001t0002g0243 others(47): Show |
50 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(47): 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 | a0001c0002t0002g0169 a0001c0002t0002g0170 a0001c0002t0002g0180 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0096 a0001c0001t0004g0005 others(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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | 54 | a0001c0001t0001g0033 a0001c0002t0001g0178 a0001c0002t0001g0184 others(51): Show |
54 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(51): 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 | a0001c0001t0003g0266 a0001c0001t0003g0270 |
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 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0001g0102 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0027g0261 |
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 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0002t0002g0149 a0001c0002t0002g0156 a0001c0002t0002g0158 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | 264 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0007g0029 a0001c0001t0007g0030 a0004c0005t0007g0031 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0001t0003g0215 a0001c0001t0003g0227 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0003g0275 a0001c0001t0003g0276 a0001c0001t0028g0277 |
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 | 266 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0002g0244 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0096 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0007 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0002g0258 a0002c0004t0001g0012 a0002c0004t0001g0013 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0008g0100 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0262 others(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 | a0001c0001t0003g0262 a0001c0001t0003g0263 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0020g0018 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0037 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0002g0258 a0001c0001t0003g0017 a0001c0001t0003g0262 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0002g0233 a0001c0002t0013g0234 |
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 | a0001c0002t0002g0161 a0001c0002t0002g0230 a0001c0002t0002g0231 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | 55 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0002t0001g0178 others(52): Show |
55 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(52): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 53 | a0001c0002t0001g0178 a0001c0002t0001g0184 a0001c0002t0002g0149 others(50): Show |
53 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(50): 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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0272 a0001c0001t0003g0273 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0258 a0001c0001t0003g0017 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | 264 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | 262 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): 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 | a0001c0001t0003g0134 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0072 others(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 | a0001c0001t0003g0203 a0001c0001t0003g0207 a0003c0008t0001g0256 |
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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0116 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0065 a0001c0001t0002g0208 a0001c0001t0008g0084 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0003g0203 a0001c0001t0003g0207 a0001c0002t0002g0209 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 others(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 | a0001c0001t0003g0017 a0001c0001t0013g0020 a0001c0001t0013g0021 others(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 | a0001c0002t0002g0193 a0001c0002t0010g0192 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | 264 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0063 a0001c0001t0001g0106 a0001c0001t0001g0111 others(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 | a0001c0001t0003g0016 a0001c0001t0014g0047 |
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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | 70 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0002g0208 others(67): Show |
70 | HG00140.hp2 HG01074.hp1 HG01106.hp2 others(67): 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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0003g0016 a0001c0001t0014g0047 |
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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0002g0132 a0001c0001t0003g0265 a0001c0001t0006g0250 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0069 a0001c0001t0001g0085 others(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 | a0001c0001t0003g0151 a0001c0001t0003g0153 a0001c0001t0003g0196 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0009 |
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 | a0001c0001t0003g0264 a0001c0001t0003g0265 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0002t0002g0149 a0001c0002t0002g0156 a0001c0002t0002g0158 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0021g0015 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0003t0016g0240 |
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 | a0001c0002t0002g0149 a0001c0002t0002g0156 a0001c0002t0002g0158 others(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 | a0001c0002t0002g0149 a0001c0002t0002g0156 a0001c0002t0002g0158 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0017 a0001c0001t0013g0020 a0001c0001t0013g0021 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0105 a0001c0001t0008g0095 a0001c0001t0042g0043 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0003g0262 a0001c0001t0003g0263 |
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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0017g0107 a0001c0001t0031g0068 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0118 a0001c0001t0003g0224 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | 73 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0086 others(70): Show |
73 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(70): 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 | a0001c0001t0001g0116 a0001c0001t0003g0274 a0001c0002t0002g0165 others(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 | a0001c0001t0001g0039 a0001c0001t0003g0150 a0001c0001t0003g0215 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0114 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0093 a0001c0001t0003g0155 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0002g0236 a0001c0002t0002g0255 |
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 | 53 | a0001c0001t0002g0035 a0001c0001t0002g0258 a0001c0002t0002g0149 others(50): Show |
53 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(50): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0007g0109 a0001c0001t0007g0110 |
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 | a0001c0001t0001g0086 a0001c0001t0003g0017 a0001c0001t0020g0018 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0003g0017 a0001c0003t0016g0240 |
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 | a0001c0001t0003g0017 a0001c0003t0016g0240 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0116 |
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 | 247 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0105 a0001c0001t0008g0095 a0001c0001t0042g0043 |
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 | 249 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): 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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0001g0065 a0001c0001t0008g0084 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0003g0151 a0001c0001t0003g0198 a0001c0001t0003g0200 |
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 | a0001c0001t0003g0264 a0001c0001t0003g0265 |
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 | a0001c0001t0003g0151 a0001c0001t0003g0198 a0001c0001t0003g0200 |
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 | 80 | a0001c0001t0001g0033 a0001c0001t0001g0098 a0001c0001t0002g0035 others(77): Show |
80 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(77): 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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0007 |
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 | 56 | a0001c0001t0001g0033 a0001c0001t0002g0035 a0001c0001t0002g0242 others(53): Show |
56 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(53): 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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0058 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0134 a0001c0001t0003g0135 others(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 | a0001c0001t0001g0034 a0001c0001t0002g0208 a0001c0001t0004g0001 others(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 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 |
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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0002t0002g0186 a0001c0002t0003g0167 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | |||||||
| chr6:108635585 | T | C | 3 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0114 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0005g0139 a0001c0001t0005g0141 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0003g0151 a0001c0001t0003g0200 |
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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0004 others(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 | 68 | a0001c0001t0001g0033 a0001c0001t0002g0035 a0001c0001t0002g0208 others(65): Show |
68 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(65): 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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | |||||||
| chr6:108639905 | A | G | 14 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0016 a0001c0001t0014g0047 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | 67 | a0001c0001t0002g0035 a0001c0001t0002g0208 a0001c0001t0002g0242 others(64): Show |
67 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(64): 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 | a0001c0001t0004g0001 a0001c0001t0004g0002 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0060 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0003g0017 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | 271 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0002g0208 a0001c0001t0010g0174 a0001c0001t0010g0189 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0244 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0006g0247 a0001c0001t0006g0248 a0001c0001t0006g0250 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0215 a0001c0001t0003g0227 |
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 | a0001c0001t0003g0017 a0001c0001t0005g0124 a0001c0001t0005g0127 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | 274 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(271): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): 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 | a0001c0001t0011g0147 a0001c0001t0011g0148 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0002c0004t0001g0013 a0002c0004t0001g0014 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0003g0275 a0001c0001t0003g0276 a0001c0001t0028g0277 |
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 | a0001c0001t0003g0203 a0001c0001t0003g0207 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0059 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0203 a0001c0001t0003g0207 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0040 |
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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0002g0244 a0001c0001t0003g0207 a0001c0001t0004g0001 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0008g0122 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
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 | a0001c0001t0015g0201 a0001c0001t0015g0217 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0026 a0001c0001t0003g0017 a0001c0001t0003g0155 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0002g0244 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0058 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0085 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0003g0221 a0001c0001t0003g0237 a0001c0001t0003g0238 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0002t0002g0149 a0001c0002t0002g0168 a0001c0002t0002g0169 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0155 a0001c0001t0003g0262 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0105 a0001c0001t0008g0095 a0001c0001t0042g0043 |
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 | |||||||
| chr6:108654261 | C | G | 53 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0021g0015 |
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 | 68 | a0001c0001t0002g0035 a0001c0001t0002g0208 a0001c0001t0002g0242 others(65): Show |
68 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(65): 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 | a0001c0001t0002g0208 a0001c0002t0002g0190 a0001c0002t0002g0193 others(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 | a0001c0001t0001g0045 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0001g0096 a0001c0001t0012g0173 a0001c0001t0012g0199 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0021g0015 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0003g0151 a0001c0001t0003g0153 a0001c0001t0003g0196 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0017g0071 a0001c0001t0017g0107 a0001c0001t0031g0068 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | 6 | a0001c0002t0002g0187 a0001c0002t0002g0188 a0001c0002t0002g0194 others(3): Show |
6 | HG00140.hp2 HG01123.hp1 HG01256.hp2 others(3): 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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0016 a0001c0001t0004g0001 a0001c0001t0004g0002 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0092 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | 247 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0065 a0001c0001t0008g0084 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0002t0002g0156 a0001c0002t0002g0160 a0001c0002t0002g0161 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | 247 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0006g0247 a0001c0001t0006g0248 a0001c0001t0034g0246 |
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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0150 a0001c0001t0003g0226 |
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 | a0001c0002t0002g0149 a0001c0002t0002g0168 a0001c0002t0002g0169 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
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 | a0001c0001t0003g0215 a0001c0001t0003g0227 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 98 | a0001c0001t0002g0035 a0001c0001t0002g0130 a0001c0001t0002g0131 others(95): Show |
98 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(95): 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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0005g0137 a0001c0002t0002g0177 |
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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0150 a0001c0001t0003g0151 others(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 | a0001c0001t0003g0016 a0001c0001t0014g0047 |
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 | a0001c0001t0011g0145 a0001c0001t0011g0146 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 |
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 | a0001c0001t0003g0204 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0001c0001t0003g0204 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0001c0001t0003g0204 a0001c0001t0003g0221 a0001c0001t0003g0237 others(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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0003g0195 a0001c0001t0003g0197 a0001c0001t0003g0205 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0099 |
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 | 273 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0002g0152 a0001c0001t0003g0017 a0001c0001t0003g0150 others(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 | 256 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0003g0155 a0001c0001t0003g0262 a0001c0001t0003g0263 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | |||||||
| chr6:108671693 | 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 | a0001c0001t0020g0018 a0001c0001t0020g0019 a0001c0001t0021g0015 |
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 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0002t0013g0234 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | a0001c0001t0003g0215 a0001c0001t0003g0227 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0098 others(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 | a0001c0001t0012g0173 a0001c0001t0012g0199 a0001c0001t0012g0202 |
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 | a0001c0001t0021g0015 a0001c0001t0040g0032 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0114 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0245 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0003g0275 a0001c0001t0003g0276 a0001c0001t0028g0277 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0011g0145 a0001c0001t0011g0146 a0001c0001t0011g0147 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0003g0216 a0001c0001t0024g0229 |
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 | 268 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0152 a0001c0001t0003g0016 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0150 others(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 | a0001c0001t0002g0152 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0098 others(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 | a0001c0001t0002g0243 a0001c0001t0006g0010 a0001c0001t0006g0245 others(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 | a0001c0001t0002g0242 a0001c0001t0006g0011 a0001c0001t0011g0147 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0003g0153 a0001c0001t0003g0204 a0001c0001t0003g0219 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | |||||||
| chr6:108679162 | C | T | 2 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0020g0018 a0001c0001t0020g0019 |
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 | a0001c0001t0002g0152 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0005g0137 others(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 | a0001c0001t0001g0065 a0001c0001t0008g0084 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 |