| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3660082-3660292 | Rare:54; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:4013448-4013796 | Common:1; Rare:95 | ||||
| chr17:4016074-4016248 | Common:1; Rare:33 | ||||
| chr17:4144299-4144610 | Common:6; Rare:76 | ||||
| chr17:4483573-4483659 | Rare:14 | ||||
| chr17:4558942-4559242 | Common:3; Rare:74 | ||||
| chr17:4881032-4881167 | Rare:33 | ||||
| chr17:4981804-4981854 | Rare:12 | ||||
| chr17:4989012-4989163 | Rare:22 | ||||
| chr17:5020321-5020670 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr17:7500790-7501045 | Common:1; Rare:57 | ||||
| chr17:7836358-7836466 | Rare:30 | ||||
| chr17:7841169-7841286 | Rare:24 | ||||
| chr17:7849928-7850158 | Rare:53 | ||||
| chr17:7903044-7903323 | Common:1; Rare:66 |