| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303724-2304025 | Common:4; Rare:173 | ||||
| chr17:2336425-2336633 | Rare:152 | ||||
| chr17:2337358-2337624 | Common:1; Rare:109 | ||||
| chr17:2337959-2338147 | Common:1; Rare:48 | ||||
| chr17:2392618-2392940 | Common:13; Rare:289 | ||||
| chr17:2393020-2393470 | Common:8; Rare:310 | ||||
| chr17:2393740-2394070 | Common:6; Rare:241 | ||||
| chr17:2396750-2397120 | Common:4; Rare:159 | ||||
| chr17:2399882-2400086 | Rare:83 | ||||
| chr17:2400949-2401267 | Rare:161 | ||||
| chr17:2401480-2401820 | Common:1; Rare:152 | ||||
| chr17:2511180-2511730 | Common:3; Rare:184 | ||||
| chr17:2511749-2512031 | Common:4; Rare:141 | ||||
| chr17:2593449-2593702 | Common:6; Rare:181; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:2593866-2594021 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):3 |