Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:94436926-94437122 | Rare:39 | ||||
chr8:94553445-94553777 | Common:3; Rare:116 | ||||
chr8:94719772-94719983 | Common:1; Rare:64 | ||||
chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
chr8:96261557-96261979 | Common:6; Rare:142 | ||||
chr8:98045345-98045666 | Common:3; Rare:97 | ||||
chr8:98117120-98117319 | Common:2; Rare:67 | ||||
chr8:99013007-99013368 | Rare:76; Clinvar:1 | ||||
chr8:100150564-100150701 | Rare:43 | ||||
chr8:100309914-100310337 | Common:1; Rare:161 | ||||
chr8:100953340-100953391 | Common:1; Rare:11 | ||||
chr8:101492296-101492452 | Common:1; Rare:27 | ||||
chr8:101492514-101492774 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chr8:102239026-102239344 | Common:4; Rare:70; Clinvar (benign):1 | ||||
chr8:102655666-102655850 | Common:1; Rare:71 |