| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7886165-7886282 | Common:1; Rare:25 | ||||
| chr17:7887412-7887826 | Common:1; Rare:83 | ||||
| chr17:7915763-7916037 | Common:5; Rare:108 | ||||
| chr17:8153645-8153791 | Common:1; Rare:22 | ||||
| chr17:8154244-8154394 | Common:1; Rare:30 | ||||
| chr17:8365454-8365590 | Rare:22 | ||||
| chr17:8480229-8480406 | Rare:63 | ||||
| chr17:8746037-8746187 | Common:2; Rare:34 | ||||
| chr17:8769245-8769412 | Common:2; Rare:35 | ||||
| chr17:8807335-8807515 | Common:1; Rare:23 | ||||
| chr17:9451989-9452150 | Common:1; Rare:31 | ||||
| chr17:9809459-9809768 | Common:10; Rare:93 | ||||
| chr17:10383061-10383173 | Common:1; Rare:22 | ||||
| chr17:10638401-10638682 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr17:10791905-10792020 | Common:1; Rare:13 |