Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74493570-74493765 | Common:3; Rare:74; Clinvar (benign):3 | ||||
chr14:77708005-77708108 | Rare:51 | ||||
chr14:94081154-94081362 | Common:3; Rare:68 | ||||
chr14:102362858-102363089 | Rare:103 | ||||
chr15:40039120-40039278 | Rare:67 | ||||
chr15:49423111-49423260 | Common:1; Rare:29 | ||||
chr15:55319094-55319187 | Common:1; Rare:25 | ||||
chr15:90233914-90234259 | Common:6; Rare:98 | ||||
chr16:2047804-2047978 | Rare:69 | ||||
chr16:8797637-8797852 | Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr16:28846316-28846606 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
chr16:56451309-56451558 | Common:1; Rare:65 | ||||
chr16:56608521-56608679 | Common:1; Rare:46 | ||||
chr16:57447359-57447493 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr16:67481105-67481380 | Common:1; Rare:96 |