Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:86563338-86563551 | Common:2; Rare:80 | ||||
chr2:86720065-86720322 | Rare:106 | ||||
chr2:88170151-88170353 | Common:6; Rare:43 | ||||
chr2:88691462-88691864 | Common:2; Rare:154; Clinvar:1 | ||||
chr2:95165650-95165828 | Rare:55 | ||||
chr2:95207445-95207542 | Rare:36 | ||||
chr2:96208205-96208427 | Rare:115 | ||||
chr2:96208666-96208954 | Common:5; Rare:105 | ||||
chr2:96265946-96266348 | Common:2; Rare:121; Clinvar:2 | ||||
chr2:96305456-96305631 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
chr2:96842603-96842892 | Rare:47 | ||||
chr2:96857911-96858258 | Common:2; Rare:129 | ||||
chr2:97663902-97664241 | Common:1; Rare:110 | ||||
chr2:98608313-98608659 | Common:1; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
chr2:99154852-99155055 | Common:2; Rare:85; Clinvar (benign):2 |