Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:41934117-41934415 | Rare:63 | ||||
chr2:55870719-55871125 | Common:1; Rare:87; Clinvar (benign):1 | ||||
chr2:70086269-70086300 | Common:1; Rare:10 | ||||
chr2:74120557-74120592 | Common:1; Rare:8 | ||||
chr2:87455343-87455599 | Common:2; Rare:53 | ||||
chr2:88016540-88016800 | Common:9; Rare:111 | ||||
chr2:89585647-89585709 | |||||
chr2:91655372-91655389 | Common:1; Rare:2 | ||||
chr2:91659914-91660021 | Rare:18 | ||||
chr2:102037782-102037980 | Common:3; Rare:38 | ||||
chr2:111494980-111495369 | Common:2; Rare:53 | ||||
chr2:120222369-120222606 | Rare:51 | ||||
chr2:126657130-126657359 | Common:2; Rare:43 | ||||
chr2:127084220-127084460 | Common:2; Rare:56 | ||||
chr2:131682260-131682533 | Common:5; Rare:64 |