Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:31420528-31420760 | Common:3; Rare:71 | ||||
chr14:31457385-31457577 | Common:2; Rare:67 | ||||
chr14:31561291-31561515 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076128-32076337 | Rare:62 | ||||
chr14:32076679-32077041 | Common:3; Rare:109 | ||||
chr14:32329211-32329379 | Rare:27 | ||||
chr14:34462226-34462548 | Common:1; Rare:107 | ||||
chr14:34539653-34539882 | Common:1; Rare:59 | ||||
chr14:34629979-34630260 | Common:5; Rare:112 | ||||
chr14:34714545-34714785 | Common:4; Rare:85 | ||||
chr14:35046148-35046466 | Common:1; Rare:106 | ||||
chr14:35122232-35122597 | Common:1; Rare:111 | ||||
chr14:35292224-35292457 | Common:3; Rare:86 | ||||
chr14:35809175-35809404 | Common:1; Rare:59 | ||||
chr14:36320580-36320687 | Common:3; Rare:42 |