Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4736389-4736520 | Rare:25 | ||||
chr17:4796027-4796234 | Common:1; Rare:70 | ||||
chr17:4806987-4807192 | Common:4; Rare:66 | ||||
chr17:4939906-4940035 | Rare:45 | ||||
chr17:4940044-4940390 | Common:1; Rare:95 | ||||
chr17:4947154-4947254 | Common:1; Rare:27 | ||||
chr17:4947900-4948034 | Rare:37 | ||||
chr17:4948942-4949177 | Common:2; Rare:82 | ||||
chr17:4967004-4967432 | Common:2; Rare:105 | ||||
chr17:4967725-4968118 | Common:1; Rare:140 | ||||
chr17:4987625-4987819 | Common:2; Rare:67 | ||||
chr17:4997998-4998154 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr17:5123099-5123420 | Rare:107 | ||||
chr17:5191838-5192112 | Common:2; Rare:88 | ||||
chr17:5234804-5234983 | Rare:39 |