| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17824066-17824464 | Common:1; Rare:52 | ||||
| chr17:17836487-17836709 | Common:1; Rare:49 | ||||
| chr17:17836825-17837216 | Common:3; Rare:91 | ||||
| chr17:18026542-18026547 | Rare:2 | ||||
| chr17:18039010-18039052 | Rare:13; Clinvar:1 | ||||
| chr17:18039100-18039534 | Common:5; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18039824-18039881 | Rare:10 | ||||
| chr17:18087704-18088057 | Rare:92 | ||||
| chr17:18088300-18088334 | Rare:8 | ||||
| chr17:18153768-18153898 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:18158195-18158353 | Common:1; Rare:35 | ||||
| chr17:18182614-18182757 | Common:1; Rare:33 | ||||
| chr17:18182883-18183180 | Common:1; Rare:80 | ||||
| chr17:18183195-18183556 | Rare:99 | ||||
| chr17:18183643-18183962 | Common:1; Rare:145 |