Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23567756-23567871 | Rare:23 | ||||
chr14:23953638-23953810 | Common:7; Rare:65 | ||||
chr14:23954129-23954349 | Common:1; Rare:61 | ||||
chr14:23988837-23988950 | Common:4; Rare:49 | ||||
chr14:24093997-24094313 | Common:4; Rare:86 | ||||
chr14:24115018-24115280 | Common:2; Rare:72 | ||||
chr14:24141586-24141862 | Rare:56 | ||||
chr14:24146543-24146751 | Rare:74 | ||||
chr14:24195410-24195696 | Common:1; Rare:68 | ||||
chr14:24213425-24213529 | Rare:37 | ||||
chr14:24232312-24232687 | Common:8; Rare:89 | ||||
chr14:24232718-24232949 | Common:1; Rare:48 | ||||
chr14:24242249-24242413 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24242559-24242743 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24263157-24263313 | Common:2; Rare:38 |