Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:95676930-95677252 | Common:4; Rare:115 | ||||
chr13:98576183-98576295 | Common:1; Rare:34 | ||||
chr13:99200668-99200933 | Common:6; Rare:125 | ||||
chr13:99307397-99307691 | Common:2; Rare:41 | ||||
chr13:100088948-100089134 | Rare:69; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596785-102597041 | Common:1; Rare:120 | ||||
chr13:102773761-102773860 | Rare:39 | ||||
chr13:108218321-108218520 | Rare:78 | ||||
chr13:110615293-110615666 | Common:3; Rare:117 | ||||
chr13:110715831-110715849 | Rare:12 | ||||
chr13:111153614-111153720 | Common:2; Rare:46 | ||||
chr13:112968266-112968472 | Rare:47 | ||||
chr13:113208614-113208751 | Rare:82 | ||||
chr13:113297071-113297279 | Rare:86 | ||||
chr13:113490699-113491043 | Common:1; Rare:124 |