Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107203582-107203850 | Common:1; Rare:67; Clinvar:1 | ||||
chr7:107298109-107298174 | Common:1; Rare:22; Clinvar (benign):2 | ||||
chr7:107395218-107395252 | Rare:4 | ||||
chr7:107924008-107924340 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):5 | ||||
chr7:108079745-108079996 | Common:3; Rare:43 | ||||
chr7:108520977-108521226 | Rare:46 | ||||
chr7:112455542-112455765 | Common:4; Rare:49 | ||||
chr7:112462172-112462379 | Common:1; Rare:61 | ||||
chr7:112776827-112777115 | Common:1; Rare:42 | ||||
chr7:112787272-112787375 | Rare:18 | ||||
chr7:116211453-116211606 | Rare:33 | ||||
chr7:116327867-116328045 | Common:1; Rare:34 | ||||
chr7:116502565-116502581 | Rare:1 | ||||
chr7:116504873-116505011 | Common:1; Rare:19 | ||||
chr7:116505756-116506002 | Common:3; Rare:54 |