Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1516588-1516962 | Common:2; Rare:130 | ||||
chr17:1628812-1628997 | Rare:64 | ||||
chr17:1684802-1685038 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr17:1829792-1830038 | Common:6; Rare:106 | ||||
chr17:2303709-2303987 | Common:2; Rare:106 | ||||
chr17:2336435-2336553 | Rare:42 | ||||
chr17:2511806-2512021 | Common:2; Rare:68 | ||||
chr17:2593460-2593690 | Common:3; Rare:88; Clinvar (benign):2 | ||||
chr17:2593861-2593998 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):3 | ||||
chr17:3636241-3636459 | Common:4; Rare:61; Clinvar (benign):1 | ||||
chr17:3668575-3668857 | Common:1; Rare:112 | ||||
chr17:3723802-3723926 | Rare:69 | ||||
chr17:4143020-4143218 | Rare:62 | ||||
chr17:4143617-4143731 | Common:4; Rare:65 | ||||
chr17:4263934-4264096 | Rare:65 |