| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14069354-14069608 | Common:2; Rare:97; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:15684232-15684337 | Common:3; Rare:37 | ||||
| chr17:15699510-15699791 | Common:3; Rare:74 | ||||
| chr17:15999566-16000189 | Common:4; Rare:257; Clinvar:6; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr17:16215530-16215657 | Common:1; Rare:52 | ||||
| chr17:16415524-16415824 | Common:4; Rare:77 | ||||
| chr17:17237130-17237452 | Common:4; Rare:97; Clinvar (benign):2 | ||||
| chr17:17281164-17281376 | Rare:84 | ||||
| chr17:17591589-17591926 | Common:2; Rare:96 | ||||
| chr17:18087807-18087985 | Rare:43 | ||||
| chr17:18254649-18254823 | Rare:55 | ||||
| chr17:18258675-18258794 | Common:1; Rare:42 | ||||
| chr17:18314921-18315317 | Common:1; Rare:110 | ||||
| chr17:18682216-18682469 | Common:9; Rare:25 | ||||
| chr17:18697973-18698034 | Common:1; Rare:16 |