Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49767371-49767451 | Rare:12 | ||||
chr14:49767506-49767711 | Common:2; Rare:77 | ||||
chr14:49852741-49852847 | Common:2; Rare:51 | ||||
chr14:49892873-49893135 | Rare:117 | ||||
chr14:50116502-50116699 | Rare:111 | ||||
chr14:50312215-50312376 | Rare:62 | ||||
chr14:50532469-50532755 | Common:3; Rare:91 | ||||
chr14:50668338-50668556 | Common:3; Rare:84 | ||||
chr14:50944315-50944565 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:51240093-51240295 | Common:1; Rare:81 | ||||
chr14:51651691-51651915 | Common:3; Rare:54 | ||||
chr14:52314034-52314333 | Common:2; Rare:77 | ||||
chr14:52552498-52552892 | Common:1; Rare:124 | ||||
chr14:52707057-52707217 | Common:1; Rare:73 | ||||
chr14:52791444-52791813 | Common:2; Rare:123 |