Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209784531-209784721 | Common:1; Rare:62 | ||||
chr1:209806030-209806291 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827874-209828061 | Common:1; Rare:51 | ||||
chr1:209937952-209938267 | Common:3; Rare:108; Clinvar (pathogenic):1 | ||||
chr1:210232855-210232956 | Common:1; Rare:33 | ||||
chr1:210237100-210237348 | Rare:40 | ||||
chr1:210328687-210328879 | Common:2; Rare:64 | ||||
chr1:210328882-210329013 | Rare:46 | ||||
chr1:210329247-210329382 | Rare:49 | ||||
chr1:211258954-211259408 | Common:3; Rare:162 | ||||
chr1:211259411-211259618 | Common:2; Rare:85 | ||||
chr1:211259726-211259975 | Rare:72 | ||||
chr1:211675589-211675762 | Rare:34 | ||||
chr1:212035497-212035769 | Common:1; Rare:72 | ||||
chr1:212285044-212285373 | Common:3; Rare:95 |