Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23953661-23953800 | Common:6; Rare:50 | ||||
chr14:23988761-23988917 | Common:8; Rare:62 | ||||
chr14:24071366-24071562 | Common:3; Rare:53 | ||||
chr14:24114921-24114930 | |||||
chr14:24114932-24115318 | Common:2; Rare:112 | ||||
chr14:24146553-24146882 | Common:1; Rare:106 | ||||
chr14:24147264-24147498 | Common:2; Rare:60 | ||||
chr14:24195390-24195739 | Common:2; Rare:77 | ||||
chr14:24213059-24213188 | Rare:24 | ||||
chr14:24232222-24232731 | Common:8; Rare:126 | ||||
chr14:24242268-24242421 | Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24242562-24242767 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271461-24271705 | Common:2; Rare:70 | ||||
chr14:24299722-24299862 | Common:4; Rare:41 | ||||
chr14:24398984-24399063 | Rare:27 |