Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203646627-203646820 | Rare:57 | ||||
chr2:203650760-203651060 | Common:4; Rare:72 | ||||
chr2:203783560-203783860 | Common:2; Rare:56 | ||||
chr2:203819692-203820092 | Common:2; Rare:124 | ||||
chr2:205975270-205975690 | Rare:87 | ||||
chr2:206085070-206085380 | Common:3; Rare:156 | ||||
chr2:207820032-207820356 | Common:1; Rare:88 | ||||
chr2:207828370-207828810 | Common:6; Rare:163 | ||||
chr2:207847853-207848257 | Common:2; Rare:138 | ||||
chr2:207869892-207870160 | Common:2; Rare:74 | ||||
chr2:207935910-207936338 | Common:1; Rare:102 | ||||
chr2:215325810-215326090 | Common:1; Rare:68; Clinvar (benign):1 | ||||
chr2:215326690-215327040 | Common:3; Rare:101 | ||||
chr2:215391432-215391980 | Common:5; Rare:216 | ||||
chr2:215423953-215424530 | Common:15; Rare:237 |