Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103385377-103385446 | Common:1; Rare:27 | ||||
chr14:103521465-103521805 | Common:2; Rare:96 | ||||
chr14:103529086-103529233 | Common:1; Rare:47 | ||||
chr14:103562233-103562356 | Rare:56 | ||||
chr14:103562620-103563100 | Common:8; Rare:190; Clinvar (benign):5 | ||||
chr14:103629111-103629451 | Common:3; Rare:136 | ||||
chr14:103715471-103715779 | Rare:79 | ||||
chr14:104752949-104753212 | Common:3; Rare:98 | ||||
chr14:104970476-104970781 | Common:4; Rare:60 | ||||
chr14:105419735-105420032 | Rare:94 | ||||
chr14:105468759-105469134 | Common:3; Rare:95 | ||||
chr14:105487032-105487270 | Common:2; Rare:77 | ||||
chr15:25438984-25439227 | Common:2; Rare:91 | ||||
chr15:29822016-29822602 | Common:2; Rare:220 | ||||
chr15:30903718-30903952 | Common:1; Rare:60 |