| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484215-7484388 | Common:1; Rare:74 | ||||
| chr17:7484690-7484828 | Rare:59 | ||||
| chr17:7499161-7499323 | Common:2; Rare:48 | ||||
| chr17:7561782-7562044 | Common:3; Rare:74 | ||||
| chr17:7570186-7570428 | Rare:43 | ||||
| chr17:7579170-7579524 | Common:1; Rare:134 | ||||
| chr17:7580210-7580490 | Common:1; Rare:86 | ||||
| chr17:7583739-7583877 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584073-7584113 | Rare:8 | ||||
| chr17:7627367-7627551 | Common:1; Rare:54 | ||||
| chr17:7627555-7627603 | Rare:14 | ||||
| chr17:7627744-7627971 | Common:3; Rare:76 | ||||
| chr17:7687462-7687569 | Rare:28 | ||||
| chr17:7844048-7844139 | Common:2; Rare:25 | ||||
| chr17:7857121-7857321 | Common:1; Rare:110 |