Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:111494682-111495195 | Common:1; Rare:88 | ||||
chr2:111534884-111535200 | Rare:49 | ||||
chr2:111947544-111947757 | Common:5; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr2:111958103-111958308 | Rare:36 | ||||
chr2:111985650-111985692 | Rare:7 | ||||
chr2:111986509-111986622 | Common:1; Rare:17 | ||||
chr2:112021685-112022001 | Common:4; Rare:57 | ||||
chr2:112022038-112022401 | Common:2; Rare:84; Clinvar:3 | ||||
chr2:112276138-112276344 | Rare:62 | ||||
chr2:113583581-113583671 | Common:1; Rare:7 | ||||
chr2:113583983-113584124 | Rare:33 | ||||
chr2:113915272-113915514 | Common:1; Rare:59 | ||||
chr2:115036156-115036294 | Common:3; Rare:20 | ||||
chr2:117128513-117128846 | Rare:70 | ||||
chr2:123546035-123546151 | Common:3; Rare:29 |