Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151365013-151365247 | Common:1; Rare:67 | ||||
chr1:153663248-153663395 | Rare:28 | ||||
chr1:154586180-154586495 | Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:154671392-154671593 | Common:1; Rare:37 | ||||
chr1:155984476-155984646 | Rare:29 | ||||
chr1:156675228-156675513 | Rare:64 | ||||
chr1:161365834-161365938 | Rare:14 | ||||
chr1:178037954-178038044 | Rare:34 | ||||
chr1:178283430-178283682 | Common:1; Rare:62 | ||||
chr1:185316216-185316354 | Rare:33 | ||||
chr1:195848238-195848510 | Common:3; Rare:69 | ||||
chr1:197201257-197201506 | Common:1; Rare:83 | ||||
chr1:200038749-200039024 | Common:1; Rare:83 | ||||
chr1:200374073-200374305 | Common:1; Rare:29 | ||||
chr1:200411753-200411920 | Common:1; Rare:29 |