Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75069471-75069689 | Common:2; Rare:54 | ||||
chr14:75127001-75127120 | Rare:38 | ||||
chr14:75278256-75278607 | Common:3; Rare:73 | ||||
chr14:75278748-75278861 | Common:1; Rare:24 | ||||
chr14:75279528-75279675 | Rare:30 | ||||
chr14:75427644-75427804 | Rare:37 | ||||
chr14:75660781-75660963 | Rare:53 | ||||
chr14:75661141-75661436 | Common:4; Rare:81 | ||||
chr14:75985704-75985798 | Rare:44; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:76151746-76151978 | Rare:86 | ||||
chr14:76762169-76762374 | Common:1; Rare:44 | ||||
chr14:76812849-76812992 | Rare:53 | ||||
chr14:77028688-77028919 | Rare:76 | ||||
chr14:77097953-77098399 | Rare:139 | ||||
chr14:77181542-77181883 | Common:2; Rare:77 |