Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25430049-25430427 | Common:13; Rare:261 | ||||
chr1:25430603-25431057 | Common:8; Rare:259 | ||||
chr1:25431154-25431782 | Common:3; Rare:223 | ||||
chr1:25543447-25543725 | Common:1; Rare:104; Clinvar:5 | ||||
chr1:25800004-25800323 | Common:2; Rare:272; Clinvar:18; Clinvar (benign):18; Clinvar (pathogenic):11 | ||||
chr1:25819714-25820263 | Common:18; Rare:394 | ||||
chr1:25858677-25859091 | Common:2; Rare:146 | ||||
chr1:25859242-25859636 | Common:9; Rare:388 | ||||
chr1:25892460-25892820 | Common:5; Rare:75 | ||||
chr1:25905427-25905710 | Common:1; Rare:154 | ||||
chr1:25906311-25906458 | Rare:59 | ||||
chr1:25906388-25906588 | Rare:141 | ||||
chr1:25997926-25998454 | Common:8; Rare:228 | ||||
chr1:26110620-26110850 | Common:3; Rare:83 | ||||
chr1:26110813-26111252 | Common:8; Rare:263 |