| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2337358-2337542 | Rare:106 | ||||
| chr17:2392672-2392918 | Common:8; Rare:185 | ||||
| chr17:2396702-2397148 | Common:6; Rare:302 | ||||
| chr17:2401016-2401368 | Common:1; Rare:186 | ||||
| chr17:2511270-2511730 | Common:1; Rare:121 | ||||
| chr17:2511774-2512026 | Common:4; Rare:146 | ||||
| chr17:2593388-2593709 | Common:8; Rare:209; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:2593713-2594007 | Common:2; Rare:109; Clinvar:8; Clinvar (benign):6 | ||||
| chr17:2710748-2710993 | Common:2; Rare:89 | ||||
| chr17:2711583-2711927 | Rare:184 | ||||
| chr17:3535470-3535830 | Rare:115 | ||||
| chr17:3636192-3636560 | Common:10; Rare:207; Clinvar (benign):4 | ||||
| chr17:3636622-3636789 | Common:2; Rare:78; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:3668552-3668874 | Common:4; Rare:233 | ||||
| chr17:3696030-3696600 | Common:4; Rare:180 |