Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9182327-9182440 | Common:1; Rare:34 | ||||
chr1:9196911-9197062 | Rare:32 | ||||
chr1:9233463-9233678 | Common:1; Rare:48 | ||||
chr1:9242695-9242868 | Common:1; Rare:41 | ||||
chr1:9244693-9245061 | Common:2; Rare:90; Clinvar (benign):1 | ||||
chr1:9687521-9687649 | Common:1; Rare:33 | ||||
chr1:11070952-11071033 | Rare:20 | ||||
chr1:12619044-12619142 | Rare:24 | ||||
chr1:15834886-15835171 | Common:2; Rare:121 | ||||
chr1:15835804-15836134 | Common:6; Rare:159 | ||||
chr1:16154728-16154821 | Common:1; Rare:10 | ||||
chr1:16155213-16155230 | Rare:4 | ||||
chr1:16208390-16208654 | Common:1; Rare:52 | ||||
chr1:16217325-16217691 | Common:2; Rare:62 | ||||
chr1:16499217-16499383 | Rare:78 |