Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24442638-24443073 | Common:6; Rare:128 | ||||
chr14:24634166-24634457 | Common:4; Rare:82 | ||||
chr14:30559055-30559201 | Common:2; Rare:54 | ||||
chr14:30622151-30622383 | Common:1; Rare:101 | ||||
chr14:31025144-31025506 | Rare:89 | ||||
chr14:31025624-31025675 | Rare:17 | ||||
chr14:31026373-31026593 | Common:3; Rare:68 | ||||
chr14:31121445-31121804 | Common:2; Rare:83 | ||||
chr14:31207107-31207226 | Rare:34 | ||||
chr14:31207463-31207570 | Rare:28 | ||||
chr14:31207590-31207926 | Common:2; Rare:113 | ||||
chr14:31420524-31420760 | Common:3; Rare:71 | ||||
chr14:31457360-31457577 | Common:2; Rare:77 | ||||
chr14:31561089-31561515 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076251-32076320 | Rare:22 |