Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96502286-96502471 | Rare:69 | ||||
chr14:99480788-99480982 | Common:2; Rare:77 | ||||
chr14:100375453-100375675 | Common:1; Rare:30 | ||||
chr14:100376269-100376495 | Common:3; Rare:76 | ||||
chr14:102139678-102139916 | Rare:82 | ||||
chr14:102362862-102363075 | Rare:100 | ||||
chr14:103333909-103334246 | Common:3; Rare:139 | ||||
chr14:103529093-103529233 | Common:1; Rare:45 | ||||
chr14:103562624-103563019 | Common:6; Rare:143; Clinvar (benign):2 | ||||
chr14:105021031-105021402 | Common:1; Rare:134 | ||||
chr15:23039546-23039746 | Common:1; Rare:80 | ||||
chr15:34101843-34102083 | Common:1; Rare:48 | ||||
chr15:36579518-36579654 | Common:2; Rare:32 | ||||
chr15:39933984-39934187 | Common:4; Rare:71 | ||||
chr15:40039103-40039320 | Rare:92 |