| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32927857-32928044 | Common:2; Rare:61 | ||||
| chr17:32928129-32928244 | Rare:33 | ||||
| chr17:32928347-32928395 | Common:1; Rare:12 | ||||
| chr17:34255129-34255285 | Rare:40 | ||||
| chr17:34960863-34961054 | Rare:38 | ||||
| chr17:34961169-34961276 | Common:1; Rare:33 | ||||
| chr17:34961311-34961653 | Common:4; Rare:149 | ||||
| chr17:34961783-34961898 | Common:1; Rare:39 | ||||
| chr17:34962130-34962453 | Rare:84 | ||||
| chr17:34980314-34981280 | Common:8; Rare:265 | ||||
| chr17:34981283-34981317 | Rare:4 | ||||
| chr17:35063544-35063889 | Rare:57 | ||||
| chr17:35089013-35089559 | Common:7; Rare:130 | ||||
| chr17:35119446-35119488 | Rare:14 | ||||
| chr17:35119506-35119785 | Rare:108; Clinvar:20; Clinvar (benign):17; Clinvar (pathogenic):2 |