Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100376263-100376521 | Common:3; Rare:84 | ||||
chr14:101809727-101809887 | Rare:33 | ||||
chr14:101810287-101810447 | Common:2; Rare:34 | ||||
chr14:102083510-102083983 | Common:4; Rare:201 | ||||
chr14:102086989-102087496 | Common:6; Rare:209 | ||||
chr14:102087539-102087614 | Common:1; Rare:20 | ||||
chr14:102139645-102139932 | Rare:102 | ||||
chr14:102362862-102363092 | Rare:103 | ||||
chr14:102928496-102928683 | Rare:65 | ||||
chr14:103123250-103123481 | Rare:41 | ||||
chr14:103333969-103334258 | Common:1; Rare:121 | ||||
chr14:103521465-103521797 | Common:2; Rare:95 | ||||
chr14:103529035-103529235 | Common:1; Rare:61 | ||||
chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:104085386-104085717 | Common:1; Rare:57 |