Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:33767190-33767312 | Rare:19 | ||||
chr14:33791995-33792226 | Rare:32 | ||||
chr14:34874172-34874206 | Common:1; Rare:11 | ||||
chr14:35986347-35986480 | Common:1; Rare:18 | ||||
chr14:35993090-35993240 | Common:1; Rare:24 | ||||
chr14:36065884-36066100 | Common:5; Rare:42 | ||||
chr14:36067211-36067284 | Rare:9 | ||||
chr14:36067696-36068096 | Common:2; Rare:75 | ||||
chr14:38004625-38004690 | Common:1; Rare:11 | ||||
chr14:38125449-38125696 | Rare:44 | ||||
chr14:49633956-49634092 | Common:1; Rare:60; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862407-49862558 | Rare:37 | ||||
chr14:49862645-49863048 | Common:1; Rare:186 | ||||
chr14:49868111-49868367 | Common:1; Rare:54 | ||||
chr14:49971323-49971477 | Rare:29 |