Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:109265142-109265419 | Common:4; Rare:64 | ||||
chr13:109272042-109272211 | Common:5; Rare:41 | ||||
chr13:110308510-110308622 | Common:1; Rare:22 | ||||
chr14:49633926-49634043 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr14:49862735-49863005 | Rare:123 | ||||
chr14:50003419-50003568 | Rare:40 | ||||
chr15:41283750-41284015 | Common:2; Rare:69 | ||||
chr15:58547373-58547649 | Common:2; Rare:56 | ||||
chr15:72199720-72199958 | Rare:45 | ||||
chr15:73927700-73927858 | Common:1; Rare:48 | ||||
chr15:82750443-82750591 | Common:2; Rare:38 | ||||
chr16:30634276-30634553 | Common:1; Rare:70 | ||||
chr16:30875350-30875467 | Rare:36 | ||||
chr16:56617389-56617560 | Common:3; Rare:36 | ||||
chr16:72664947-72665133 | Common:1; Rare:52 |