Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216694511-216694858 | Rare:89 | ||||
chr2:217905401-217905638 | Rare:45 | ||||
chr2:217937099-217937235 | Common:4; Rare:24 | ||||
chr2:217937246-217937341 | Common:1; Rare:22 | ||||
chr2:217937517-217937758 | Rare:51 | ||||
chr2:217943863-217944136 | Rare:56 | ||||
chr2:217978622-217978713 | Rare:25 | ||||
chr2:217978769-217978965 | Common:1; Rare:61 | ||||
chr2:218217058-218217246 | Common:1; Rare:67 | ||||
chr2:218270054-218270559 | Common:5; Rare:159; Clinvar:4; Clinvar (benign):1 | ||||
chr2:218279017-218279287 | Common:2; Rare:76 | ||||
chr2:218287250-218287476 | Common:1; Rare:39 | ||||
chr2:218289992-218290219 | Common:3; Rare:38 | ||||
chr2:218381879-218382040 | Common:3; Rare:33 | ||||
chr2:218382066-218382371 | Rare:60 |