| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999575-15999824 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:16415727-16415824 | Common:1; Rare:25 | ||||
| chr17:17237396-17237677 | Common:4; Rare:64 | ||||
| chr17:17591595-17591923 | Common:1; Rare:93 | ||||
| chr17:18087771-18088008 | Rare:67 | ||||
| chr17:18183532-18183888 | Common:1; Rare:140 | ||||
| chr17:18254649-18254824 | Rare:56 | ||||
| chr17:18314928-18315308 | Common:1; Rare:107 | ||||
| chr17:18682218-18682469 | Common:9; Rare:25 | ||||
| chr17:18857935-18858175 | Common:5; Rare:58 | ||||
| chr17:19648611-19648833 | Common:3; Rare:76 | ||||
| chr17:19977804-19978139 | Common:2; Rare:93 | ||||
| chr17:21214144-21214359 | Common:2; Rare:97 | ||||
| chr17:21214593-21214696 | Common:1; Rare:32 | ||||
| chr17:27294002-27294132 | Common:1; Rare:52 |