| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4366610-4366756 | Common:1; Rare:60 | ||||
| chr17:4533069-4533369 | Rare:132 | ||||
| chr17:4544863-4545137 | Common:10; Rare:156 | ||||
| chr17:4545402-4545757 | Common:6; Rare:116 | ||||
| chr17:4555320-4555655 | Common:3; Rare:139 | ||||
| chr17:4560517-4560846 | Common:4; Rare:79 | ||||
| chr17:4704077-4704223 | Rare:79 | ||||
| chr17:4738441-4738627 | Common:2; Rare:37 | ||||
| chr17:4739508-4739584 | Common:2; Rare:20 | ||||
| chr17:4806996-4807210 | Common:4; Rare:67 | ||||
| chr17:4833259-4833652 | Common:1; Rare:94 | ||||
| chr17:4884834-4884998 | Rare:26 | ||||
| chr17:4899383-4899460 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:4939827-4940380 | Common:2; Rare:161 | ||||
| chr17:4942929-4943266 | Common:1; Rare:124 |