Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26345828-26346176 | Common:1; Rare:101 | ||||
chr2:27032831-27033049 | Rare:85 | ||||
chr2:27078762-27078915 | Common:1; Rare:28 | ||||
chr2:27211924-27212022 | Common:3; Rare:39 | ||||
chr2:27212225-27212366 | Common:1; Rare:76 | ||||
chr2:27312585-27312770 | Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
chr2:27356754-27357060 | Rare:85 | ||||
chr2:27370278-27370657 | Common:1; Rare:158 | ||||
chr2:27628977-27629100 | Common:1; Rare:68 | ||||
chr2:27663592-27663911 | Rare:113 | ||||
chr2:27771607-27771778 | Common:1; Rare:63 | ||||
chr2:27890354-27890809 | Common:1; Rare:125 | ||||
chr2:28751497-28751884 | Common:4; Rare:173 | ||||
chr2:28894354-28894657 | Common:5; Rare:92 | ||||
chr2:32039753-32039893 | Rare:43 |