Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:74627415-74627572 | Common:2; Rare:48 | ||||
chr15:74781968-74782114 | Common:3; Rare:46 | ||||
chr15:74842613-74842780 | Rare:40 | ||||
chr15:74872967-74873109 | Rare:31 | ||||
chr15:74889703-74890080 | Rare:100; Clinvar (pathogenic):1 | ||||
chr15:74906760-74906871 | Common:1; Rare:46 | ||||
chr15:74937966-74938134 | Rare:53 | ||||
chr15:74957062-74957292 | Common:1; Rare:68 | ||||
chr15:74995324-74995634 | Common:7; Rare:115 | ||||
chr15:75201767-75201924 | Common:1; Rare:56 | ||||
chr15:75335973-75336089 | Common:1; Rare:51 | ||||
chr15:75347032-75347085 | Rare:8 | ||||
chr15:75347520-75347942 | Common:2; Rare:107 | ||||
chr15:75348675-75349026 | Rare:113 | ||||
chr15:75368329-75368557 | Rare:84 |