Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:32693490-32693772 | Common:6; Rare:80 | ||||
chr19:33176841-33177053 | Common:8; Rare:103 | ||||
chr19:33300641-33300838 | Rare:42 | ||||
chr19:33301605-33301740 | Common:1; Rare:45; Clinvar:8; Clinvar (benign):8 | ||||
chr19:34173303-34173488 | Common:2; Rare:32 | ||||
chr19:35488342-35488449 | Rare:25 | ||||
chr19:35488643-35488876 | Common:3; Rare:79 | ||||
chr19:35504777-35505105 | Rare:49 | ||||
chr19:35507253-35507554 | Common:2; Rare:59 | ||||
chr19:35509154-35509468 | Common:2; Rare:64 | ||||
chr19:35526448-35526761 | Common:5; Rare:103 | ||||
chr19:35526764-35527522 | Common:5; Rare:262 | ||||
chr19:36797259-36797546 | Rare:61 | ||||
chr19:38135129-38135454 | Common:5; Rare:59 | ||||
chr19:38151358-38151377 |