Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:208615-209041 | Common:2; Rare:149 | ||||
chr11:236324-236512 | Common:6; Rare:60 | ||||
chr11:236919-237035 | Common:1; Rare:44 | ||||
chr11:506646-506987 | Common:3; Rare:104 | ||||
chr11:507135-507537 | Common:4; Rare:134 | ||||
chr11:535426-535732 | Common:5; Rare:123; Clinvar (benign):1 | ||||
chr11:537274-537546 | Common:5; Rare:83 | ||||
chr11:560707-560994 | Common:6; Rare:133 | ||||
chr11:576412-576509 | Rare:34 | ||||
chr11:695020-695351 | Common:1; Rare:79 | ||||
chr11:695615-695825 | Rare:53 | ||||
chr11:706535-706645 | Rare:19 | ||||
chr11:777458-777614 | Common:1; Rare:68 | ||||
chr11:809777-810040 | Common:2; Rare:118 | ||||
chr11:832824-833022 | Common:7; Rare:67 |