| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8248034-8248182 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:8249001-8249343 | Common:2; Rare:121 | ||||
| chr17:8295310-8295790 | Common:2; Rare:165 | ||||
| chr17:8383080-8383490 | Common:1; Rare:209 | ||||
| chr17:8435666-8436046 | Common:9; Rare:266 | ||||
| chr17:8630658-8631098 | Common:2; Rare:187 | ||||
| chr17:9644401-9644867 | Common:8; Rare:146 | ||||
| chr17:9645320-9645580 | Rare:116 | ||||
| chr17:10697477-10697660 | Common:8; Rare:166; Clinvar:10; Clinvar (benign):6 | ||||
| chr17:11997373-11997607 | Rare:147 | ||||
| chr17:13017925-13018294 | Common:11; Rare:218; Clinvar (benign):4 | ||||
| chr17:13601906-13602185 | Common:3; Rare:86 | ||||
| chr17:14069329-14069593 | Common:4; Rare:158; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:14300731-14301299 | Common:9; Rare:254 | ||||
| chr17:15563427-15563787 | Common:2; Rare:231 |