| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2511806-2511923 | Common:2; Rare:33 | ||||
| chr17:2593453-2593683 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr17:2593863-2593987 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:3636281-3636517 | Common:4; Rare:55; Clinvar (benign):1 | ||||
| chr17:3668533-3668881 | Common:3; Rare:141 | ||||
| chr17:3723758-3723922 | Common:1; Rare:91 | ||||
| chr17:4142998-4143249 | Rare:84 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263943-4264065 | Rare:49 | ||||
| chr17:4555312-4555503 | Common:3; Rare:88 | ||||
| chr17:4704104-4704250 | Rare:79 | ||||
| chr17:4731283-4731486 | Common:2; Rare:63 | ||||
| chr17:4739537-4739635 | Rare:27 | ||||
| chr17:4806987-4807192 | Common:4; Rare:66 | ||||
| chr17:4833173-4833509 | Rare:96 |