| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7857911-7858068 | Rare:55 | ||||
| chr17:7931869-7932248 | Common:5; Rare:100 | ||||
| chr17:8152378-8152567 | Common:2; Rare:44 | ||||
| chr17:8156509-8156821 | Common:1; Rare:84 | ||||
| chr17:8162887-8163082 | Rare:61 | ||||
| chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249024-8249317 | Common:1; Rare:63 | ||||
| chr17:8435706-8436006 | Common:4; Rare:120 | ||||
| chr17:8867670-8867775 | Common:1; Rare:18 | ||||
| chr17:8965674-8965884 | Common:2; Rare:56 | ||||
| chr17:10059777-10060025 | Common:2; Rare:45 | ||||
| chr17:10697430-10697654 | Common:3; Rare:101; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729745-10729807 | Rare:33 | ||||
| chr17:10729966-10730099 | Common:3; Rare:33 | ||||
| chr17:14069349-14069558 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 |