| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4717402-4717752 | Common:2; Rare:73 | ||||
| chr17:4731350-4731500 | Common:2; Rare:53 | ||||
| chr17:4731645-4731775 | Rare:44 | ||||
| chr17:4736338-4736524 | Rare:38 | ||||
| chr17:4738425-4738552 | Common:1; Rare:29 | ||||
| chr17:4739330-4739474 | Common:3; Rare:52 | ||||
| chr17:4739485-4739854 | Common:6; Rare:82 | ||||
| chr17:4739856-4740015 | Rare:37 | ||||
| chr17:4786329-4786486 | Rare:38 | ||||
| chr17:4806996-4807223 | Common:4; Rare:70 | ||||
| chr17:4833105-4833534 | Common:1; Rare:114 | ||||
| chr17:4833536-4833627 | Common:1; Rare:19 | ||||
| chr17:4893888-4894007 | Rare:25 | ||||
| chr17:4899260-4899470 | Common:1; Rare:143; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:4932119-4932293 | Rare:37 |