Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:13638904-13639112 | Common:2; Rare:73 | ||||
chr20:13784893-13785053 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr20:17968472-17968641 | Common:4; Rare:82 | ||||
chr20:17968778-17969119 | Common:4; Rare:123 | ||||
chr20:18567245-18567491 | Common:4; Rare:88 | ||||
chr20:20017162-20017396 | Rare:76 | ||||
chr20:21303231-21303385 | Rare:60 | ||||
chr20:24992698-24992815 | Common:3; Rare:55 | ||||
chr20:25696807-25697062 | Common:3; Rare:75 | ||||
chr20:31547278-31547438 | Rare:40 | ||||
chr20:31722791-31722952 | Rare:41 | ||||
chr20:31723527-31723756 | Common:1; Rare:69 | ||||
chr20:31739107-31739357 | Common:1; Rare:63 | ||||
chr20:32207710-32207944 | Common:3; Rare:92 | ||||
chr20:33401476-33401618 | Rare:37 |