Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:39174972-39175282 | Common:4; Rare:108 | ||||
chr14:39267073-39267439 | Common:1; Rare:135 | ||||
chr14:39432420-39432657 | Common:6; Rare:81 | ||||
chr14:44961892-44962258 | Common:3; Rare:106 | ||||
chr14:45253088-45253310 | Rare:58 | ||||
chr14:49586289-49586692 | Common:1; Rare:197; Clinvar (benign):1 | ||||
chr14:49598281-49598482 | Rare:54 | ||||
chr14:49598663-49599023 | Common:2; Rare:136 | ||||
chr14:49620573-49620820 | Common:2; Rare:98; Clinvar:1 | ||||
chr14:49688201-49688439 | Common:4; Rare:71 | ||||
chr14:49852761-49853130 | Common:3; Rare:91 | ||||
chr14:49892913-49893105 | Rare:76 | ||||
chr14:50116557-50116696 | Rare:63 | ||||
chr14:50312197-50312374 | Rare:67 | ||||
chr14:50532488-50532755 | Common:3; Rare:86 |