| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15260787-15260961 | Common:1; Rare:57 | ||||
| chr17:15262493-15262657 | Rare:42 | ||||
| chr17:15563439-15563707 | Rare:96 | ||||
| chr17:15684273-15684334 | Common:1; Rare:25 | ||||
| chr17:15699484-15699773 | Common:3; Rare:77 | ||||
| chr17:15999566-16000028 | Common:3; Rare:195; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217085-16217240 | Rare:42; Clinvar:1 | ||||
| chr17:16381325-16381429 | Rare:50 | ||||
| chr17:16653810-16654041 | Rare:59 | ||||
| chr17:17281194-17281321 | Rare:59 | ||||
| chr17:17476872-17477044 | Common:3; Rare:53 | ||||
| chr17:17496388-17496546 | Rare:38 | ||||
| chr17:17591595-17591894 | Common:1; Rare:89 | ||||
| chr17:17823606-17823821 | Common:5; Rare:97 | ||||
| chr17:18039092-18039437 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 |