| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7688098-7688534 | Common:5; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:7704973-7705253 | Common:2; Rare:60 | ||||
| chr17:7717340-7717399 | Common:1; Rare:10 | ||||
| chr17:7839335-7839531 | Rare:32 | ||||
| chr17:7843580-7843801 | Rare:81 | ||||
| chr17:7843907-7844219 | Common:5; Rare:94 | ||||
| chr17:7844577-7844629 | Rare:9 | ||||
| chr17:7844694-7845051 | Common:2; Rare:107 | ||||
| chr17:7856843-7857074 | Rare:88 | ||||
| chr17:7857094-7857368 | Common:1; Rare:138 | ||||
| chr17:7857451-7857746 | Common:2; Rare:95 | ||||
| chr17:7857859-7858025 | Rare:61 | ||||
| chr17:7888413-7888474 | Rare:12 | ||||
| chr17:7931873-7932267 | Common:5; Rare:106 | ||||
| chr17:8016007-8016150 | Rare:41 |