Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207052957-207053281 | Common:1; Rare:82 | ||||
chr1:207321755-207321821 | Rare:18 | ||||
chr1:207322127-207322281 | Rare:48 | ||||
chr1:207496066-207496261 | Rare:37 | ||||
chr1:207751920-207752215 | Common:1; Rare:96; Clinvar:1 | ||||
chr1:208244250-208244502 | Common:1; Rare:77 | ||||
chr1:209652423-209652571 | Rare:37; Clinvar:1 | ||||
chr1:209675280-209675453 | Common:1; Rare:42 | ||||
chr1:209784521-209784679 | Rare:50 | ||||
chr1:209937947-209938265 | Common:3; Rare:111; Clinvar (pathogenic):1 | ||||
chr1:210237047-210237355 | Rare:49 | ||||
chr1:211259733-211259995 | Rare:75 | ||||
chr1:211675588-211675746 | Rare:31 | ||||
chr1:211830636-211830903 | Common:1; Rare:69 | ||||
chr1:212035510-212035801 | Common:2; Rare:77 |