Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23095457-23095567 | Common:2; Rare:43 | ||||
chr14:23154385-23154520 | Common:3; Rare:37 | ||||
chr14:23306670-23306872 | Common:1; Rare:47 | ||||
chr14:23953638-23953770 | Common:4; Rare:48 | ||||
chr14:24094061-24094343 | Common:3; Rare:68 | ||||
chr14:24146551-24146881 | Common:1; Rare:107 | ||||
chr14:24195426-24195709 | Common:1; Rare:65 | ||||
chr14:24232312-24232687 | Common:8; Rare:89 | ||||
chr14:24242580-24242760 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271503-24271692 | Common:2; Rare:49 | ||||
chr14:24299709-24299850 | Common:4; Rare:41 | ||||
chr14:24442765-24443013 | Common:5; Rare:71 | ||||
chr14:31420528-31420737 | Common:3; Rare:66 | ||||
chr14:31561089-31561442 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:34462281-34462593 | Common:1; Rare:94 |