Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22929349-22929609 | Rare:60 | ||||
chr14:23555950-23556343 | Common:4; Rare:102 | ||||
chr14:23953638-23953810 | Common:7; Rare:65 | ||||
chr14:23988786-23988917 | Common:7; Rare:52 | ||||
chr14:24115008-24115280 | Common:2; Rare:76 | ||||
chr14:24146578-24146895 | Common:1; Rare:99 | ||||
chr14:24195400-24195727 | Common:2; Rare:73 | ||||
chr14:24232317-24232470 | Common:6; Rare:38 | ||||
chr14:24232674-24232942 | Common:1; Rare:55 | ||||
chr14:24242584-24242743 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271488-24271611 | Common:1; Rare:33 | ||||
chr14:24299738-24299850 | Common:4; Rare:31 | ||||
chr14:24442755-24443023 | Common:5; Rare:77 | ||||
chr14:30559047-30559158 | Common:2; Rare:38 | ||||
chr14:34462198-34462558 | Common:1; Rare:130 |