| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68457862-68457961 | Common:2; Rare:34 | ||||
| chr17:68511805-68512082 | Rare:69 | ||||
| chr17:68512244-68512551 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68512589-68512755 | Rare:52 | ||||
| chr17:68512946-68513024 | Common:2; Rare:22 | ||||
| chr17:68513032-68513046 | Rare:4 | ||||
| chr17:68513322-68513353 | Rare:3 | ||||
| chr17:69060925-69061148 | Common:2; Rare:36 | ||||
| chr17:69141757-69141798 | Rare:5 | ||||
| chr17:69141841-69142116 | Common:2; Rare:52 | ||||
| chr17:69175772-69176073 | Common:1; Rare:58 | ||||
| chr17:69327047-69327435 | Common:2; Rare:125 | ||||
| chr17:69414495-69414708 | Rare:39 | ||||
| chr17:69501676-69501755 | Rare:24 | ||||
| chr17:69502160-69502406 | Rare:49 |