| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7226257-7226419 | Rare:52 | ||||
| chr17:7500713-7501107 | Common:2; Rare:91 | ||||
| chr17:7836331-7836455 | Common:1; Rare:39 | ||||
| chr17:7849868-7850158 | Rare:69 | ||||
| chr17:7887415-7887819 | Common:1; Rare:81 | ||||
| chr17:7905918-7906207 | Common:3; Rare:88 | ||||
| chr17:7910623-7910901 | Common:3; Rare:84 | ||||
| chr17:7915710-7916046 | Common:5; Rare:128 | ||||
| chr17:7916207-7916319 | Rare:33 | ||||
| chr17:8047305-8047642 | Common:4; Rare:101 | ||||
| chr17:8070553-8070750 | Rare:26 | ||||
| chr17:8070842-8070901 | Common:3; Rare:5 | ||||
| chr17:8071503-8071990 | Common:3; Rare:93 | ||||
| chr17:8072111-8072323 | Common:1; Rare:28 | ||||
| chr17:8075480-8075688 | Common:1; Rare:58; Clinvar:2; Clinvar (pathogenic):3 |