| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484226-7484370 | Common:1; Rare:59 | ||||
| chr17:7583517-7583858 | Common:1; Rare:136; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7627799-7627969 | Common:2; Rare:57 | ||||
| chr17:7687465-7687554 | Rare:20 | ||||
| chr17:7857170-7857453 | Common:2; Rare:136 | ||||
| chr17:7857459-7857711 | Common:2; Rare:80 | ||||
| chr17:7931875-7932202 | Common:5; Rare:89 | ||||
| chr17:8162917-8163082 | Rare:51 | ||||
| chr17:8176343-8176471 | Rare:38 | ||||
| chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10729486-10729822 | Common:4; Rare:120 | ||||
| chr17:10729974-10730128 | Common:3; Rare:34 | ||||
| chr17:13017969-13018294 | Common:6; Rare:99; Clinvar (benign):1 | ||||
| chr17:14069395-14069580 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):3 |