Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49598670-49599038 | Common:2; Rare:141 | ||||
chr14:49620573-49620886 | Common:2; Rare:121; Clinvar:4 | ||||
chr14:49688188-49688266 | Rare:29 | ||||
chr14:49692974-49693185 | Common:1; Rare:74 | ||||
chr14:49768002-49768277 | Common:2; Rare:102 | ||||
chr14:49800893-49801173 | Common:1; Rare:43 | ||||
chr14:49892882-49893142 | Rare:114 | ||||
chr14:50116557-50116695 | Rare:63 | ||||
chr14:50312153-50312374 | Rare:96 | ||||
chr14:50396730-50396999 | Common:5; Rare:80 | ||||
chr14:50532455-50532672 | Common:3; Rare:63 | ||||
chr14:50668327-50668556 | Common:3; Rare:85 | ||||
chr14:50831026-50831281 | Common:1; Rare:89 | ||||
chr14:50831472-50831555 | Rare:18 | ||||
chr14:50944261-50944590 | Common:5; Rare:117; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 |