Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161166268-161166511 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161749749-161749837 | Rare:37 | ||||
chr1:161750205-161750460 | Rare:55 | ||||
chr1:161766225-161766376 | Common:3; Rare:49 | ||||
chr1:162497761-162497868 | Common:1; Rare:41 | ||||
chr1:162790447-162790789 | Common:4; Rare:90 | ||||
chr1:163202892-163203223 | Common:1; Rare:61 | ||||
chr1:163321752-163322130 | Common:1; Rare:95 | ||||
chr1:165768772-165768955 | Common:2; Rare:82 | ||||
chr1:166839292-166839522 | Rare:69 | ||||
chr1:167935901-167936266 | Common:1; Rare:101 | ||||
chr1:168225712-168226056 | Common:3; Rare:111 | ||||
chr1:169367739-169368250 | Common:3; Rare:107 | ||||
chr1:169794890-169795108 | Common:3; Rare:60 | ||||
chr1:170532036-170532217 | Rare:83; Clinvar:1 |