| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3658154-3658451 | Common:6; Rare:86 | ||||
| chr17:3663965-3663992 | Rare:3 | ||||
| chr17:3664196-3664351 | Common:2; Rare:31; Clinvar (pathogenic):1 | ||||
| chr17:4500012-4500330 | Common:1; Rare:60 | ||||
| chr17:4540696-4540975 | Common:5; Rare:74 | ||||
| chr17:4719928-4720231 | Common:3; Rare:80 | ||||
| chr17:4886241-4886542 | Common:1; Rare:59 | ||||
| chr17:4970511-4970590 | Rare:25 | ||||
| chr17:4982263-4982429 | Common:1; Rare:31 | ||||
| chr17:4999761-4999969 | Rare:39; Clinvar (benign):1 | ||||
| chr17:5004434-5004645 | Rare:66; Clinvar (benign):2 | ||||
| chr17:5020429-5020524 | Common:2; Rare:22; Clinvar (benign):2 | ||||
| chr17:5381218-5381469 | Common:5; Rare:54 | ||||
| chr17:5434874-5435233 | Common:2; Rare:79 | ||||
| chr17:7311015-7311481 | Rare:110 |