| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15262460-15262669 | Rare:48 | ||||
| chr17:15265284-15265447 | Rare:29; Clinvar:1 | ||||
| chr17:15563421-15563787 | Common:1; Rare:128 | ||||
| chr17:15699506-15699797 | Common:3; Rare:79 | ||||
| chr17:15999593-16000032 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039767-16039860 | Common:1; Rare:25 | ||||
| chr17:16040440-16040792 | Common:2; Rare:60 | ||||
| chr17:16215532-16215639 | Common:1; Rare:47 | ||||
| chr17:16217094-16217240 | Rare:42; Clinvar:1 | ||||
| chr17:16380593-16380814 | Common:4; Rare:55 | ||||
| chr17:16415749-16415824 | Rare:18 | ||||
| chr17:17237390-17237677 | Common:4; Rare:65 | ||||
| chr17:17281182-17281357 | Rare:71 | ||||
| chr17:17496144-17496210 | Rare:23 | ||||
| chr17:17496370-17496513 | Rare:36 |