Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2563060-2563238 | Common:2; Rare:39 | ||||
chr17:2563281-2563437 | Common:1; Rare:42 | ||||
chr17:4858937-4859167 | Common:1; Rare:52 | ||||
chr17:5004432-5004595 | Rare:56; Clinvar (benign):1 | ||||
chr17:6657091-6657357 | Common:5; Rare:28 | ||||
chr17:7311024-7311437 | Rare:102 | ||||
chr17:7435994-7436193 | Common:2; Rare:77 | ||||
chr17:7478463-7478550 | Rare:20 | ||||
chr17:7885917-7886186 | Common:3; Rare:55 | ||||
chr17:7887552-7887802 | Rare:56 | ||||
chr17:16438658-16439064 | Common:1; Rare:103 | ||||
chr17:16439401-16439506 | Common:2; Rare:38 | ||||
chr17:16822543-16822832 | Common:5; Rare:28 | ||||
chr17:17836190-17836418 | Common:3; Rare:62 | ||||
chr17:18449889-18450183 | Common:2; Rare:36 |