Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101964238-101964674 | Common:5; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
chr14:102084413-102084843 | Common:1; Rare:162 | ||||
chr14:102139671-102139923 | Rare:87 | ||||
chr14:102240587-102240770 | Common:4; Rare:30 | ||||
chr14:102305071-102305310 | Common:1; Rare:74 | ||||
chr14:102362858-102363096 | Rare:106 | ||||
chr14:103333924-103334252 | Common:3; Rare:139 | ||||
chr14:103528981-103529243 | Common:1; Rare:73 | ||||
chr14:103562620-103563074 | Common:8; Rare:179; Clinvar (benign):5 | ||||
chr14:103715489-103715853 | Common:1; Rare:117 | ||||
chr14:104970476-104970595 | Common:3; Rare:20 | ||||
chr14:105021031-105021387 | Common:1; Rare:127 | ||||
chr14:105419733-105420027 | Rare:89 | ||||
chr15:25439001-25439245 | Common:2; Rare:93 | ||||
chr15:30903732-30903946 | Common:1; Rare:55 |