Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:289000-289138 | Rare:39 | ||||
chr11:417349-417480 | Rare:33 | ||||
chr11:506743-507001 | Common:3; Rare:86 | ||||
chr11:507133-507576 | Common:4; Rare:145 | ||||
chr11:560703-561016 | Common:6; Rare:145 | ||||
chr11:576426-576515 | Rare:33 | ||||
chr11:695557-695827 | Common:1; Rare:69 | ||||
chr11:706048-706256 | Common:2; Rare:69 | ||||
chr11:747252-747493 | Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777465-777607 | Common:1; Rare:62 | ||||
chr11:809516-809647 | Common:2; Rare:33 | ||||
chr11:818701-818937 | Rare:51 | ||||
chr11:827114-827322 | Common:2; Rare:55 | ||||
chr11:832833-833014 | Common:7; Rare:61 | ||||
chr11:842454-842984 | Common:8; Rare:218 |