Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:109459588-109459908 | Common:2; Rare:56 | ||||
chr2:113325372-113325495 | Rare:18 | ||||
chr2:113541240-113541636 | Common:9; Rare:86 | ||||
chr2:120867344-120867485 | Common:1; Rare:27 | ||||
chr2:131682421-131682533 | Common:3; Rare:36 | ||||
chr2:132347338-132347481 | Common:1; Rare:37 | ||||
chr2:144513760-144513911 | Rare:46 | ||||
chr2:149571141-149571215 | Rare:22; Clinvar (benign):1 | ||||
chr2:152390065-152390263 | Rare:38 | ||||
chr2:152637496-152637672 | Rare:48 | ||||
chr2:159764376-159764658 | Rare:66 | ||||
chr2:170770771-170771101 | Common:2; Rare:57 | ||||
chr2:174436314-174436588 | Rare:60 | ||||
chr2:176637538-176637746 | Common:2; Rare:69 | ||||
chr2:177234140-177234360 | Rare:59; Clinvar:2 |