Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:33410901-33411077 | Rare:35 | ||||
chr6:33417869-33418495 | Common:3; Rare:181 | ||||
chr6:33420043-33420301 | Rare:53; Clinvar (benign):1 | ||||
chr6:33454393-33454612 | Rare:63 | ||||
chr6:33620229-33620273 | Rare:6 | ||||
chr6:33789114-33789155 | Rare:36 | ||||
chr6:34236629-34236906 | Common:3; Rare:127 | ||||
chr6:34392265-34392527 | Rare:102 | ||||
chr6:34696530-34696982 | Common:1; Rare:119 | ||||
chr6:34757138-34757550 | Common:3; Rare:88 | ||||
chr6:34887935-34888122 | Common:1; Rare:48 | ||||
chr6:35058103-35058286 | Rare:33 | ||||
chr6:35214067-35214385 | Common:2; Rare:80 | ||||
chr6:35259357-35259778 | Common:3; Rare:134 | ||||
chr6:35468095-35468456 | Common:4; Rare:105 |