Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24242556-24242774 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271457-24271831 | Common:2; Rare:100 | ||||
chr14:24299672-24299862 | Common:4; Rare:53 | ||||
chr14:24429660-24430113 | Common:3; Rare:103 | ||||
chr14:24430436-24430744 | Common:1; Rare:55 | ||||
chr14:24430980-24431232 | Common:2; Rare:55 | ||||
chr14:24442666-24443044 | Common:5; Rare:118 | ||||
chr14:30622190-30622353 | Rare:60 | ||||
chr14:30874420-30874565 | Rare:54 | ||||
chr14:32076871-32077041 | Common:2; Rare:69 | ||||
chr14:34018664-34018761 | Rare:14 | ||||
chr14:34629932-34630224 | Common:5; Rare:116 | ||||
chr14:34714570-34714759 | Common:3; Rare:72 | ||||
chr14:34875336-34875586 | Common:1; Rare:82 | ||||
chr14:34982436-34982709 | Common:1; Rare:118 |