Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:92121667-92121983 | Common:4; Rare:105 | ||||
chr14:93184867-93185008 | Rare:44 | ||||
chr14:93207038-93207281 | Common:2; Rare:120 | ||||
chr14:94081154-94081349 | Common:3; Rare:65 | ||||
chr14:96363369-96363543 | Common:1; Rare:57 | ||||
chr14:96502265-96502425 | Common:1; Rare:63 | ||||
chr14:100376277-100376424 | Common:1; Rare:50 | ||||
chr14:102139678-102139914 | Rare:80 | ||||
chr14:102362858-102363069 | Rare:99 | ||||
chr14:103562624-103563015 | Common:6; Rare:140; Clinvar (benign):2 | ||||
chr14:103715489-103715833 | Common:1; Rare:106 | ||||
chr15:34101843-34101958 | Rare:31 | ||||
chr15:34210026-34210207 | Common:2; Rare:66 | ||||
chr15:34988256-34988365 | Rare:49 | ||||
chr15:36579518-36579722 | Common:3; Rare:53 |