Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101964377-101964670 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr14:102083566-102083934 | Common:3; Rare:152 | ||||
chr14:102086984-102087377 | Common:5; Rare:166 | ||||
chr14:102087586-102087594 | Rare:2 | ||||
chr14:102139289-102139444 | Rare:68 | ||||
chr14:102139662-102139953 | Rare:102 | ||||
chr14:102240538-102240784 | Common:6; Rare:39 | ||||
chr14:102305056-102305305 | Common:1; Rare:76 | ||||
chr14:102362843-102363092 | Rare:114 | ||||
chr14:103333924-103334252 | Common:3; Rare:139 | ||||
chr14:103385077-103385452 | Common:1; Rare:109 | ||||
chr14:103529058-103529235 | Common:1; Rare:51 | ||||
chr14:103562624-103563080 | Common:8; Rare:180; Clinvar (benign):5 | ||||
chr14:103715437-103715851 | Common:1; Rare:140 | ||||
chr14:104970471-104970798 | Common:4; Rare:62 |