| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27293958-27294195 | Common:2; Rare:95 | ||||
| chr17:27294289-27294392 | Common:1; Rare:32 | ||||
| chr17:28335371-28335832 | Common:1; Rare:110 | ||||
| chr17:28357319-28357663 | Common:11; Rare:154 | ||||
| chr17:28598994-28599125 | Common:1; Rare:36 | ||||
| chr17:28645106-28645338 | Common:1; Rare:88 | ||||
| chr17:28661877-28662295 | Common:1; Rare:149 | ||||
| chr17:28718144-28718318 | Rare:52 | ||||
| chr17:28842737-28842885 | Common:1; Rare:54 | ||||
| chr17:28855006-28855032 | Rare:5 | ||||
| chr17:29140368-29140484 | Common:3; Rare:38 | ||||
| chr17:29294098-29294452 | Common:3; Rare:130 | ||||
| chr17:29568514-29568752 | Common:2; Rare:80 | ||||
| chr17:30906200-30906327 | Common:1; Rare:41 | ||||
| chr17:31095187-31095318 | Rare:49; Clinvar:3; Clinvar (benign):2 |