| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4997818-4998149 | Common:2; Rare:133; Clinvar (benign):1 | ||||
| chr17:5191833-5192101 | Common:2; Rare:86 | ||||
| chr17:5282083-5282341 | Common:11; Rare:132 | ||||
| chr17:5419368-5419406 | Rare:12 | ||||
| chr17:5419582-5419910 | Common:5; Rare:110 | ||||
| chr17:5420093-5420218 | Rare:52 | ||||
| chr17:5433009-5433401 | Common:1; Rare:122; Clinvar (pathogenic):2 | ||||
| chr17:5438847-5439089 | Common:1; Rare:85 | ||||
| chr17:5468898-5469091 | Common:2; Rare:66 | ||||
| chr17:5486009-5486608 | Common:6; Rare:201 | ||||
| chr17:5486805-5486925 | Common:4; Rare:38 | ||||
| chr17:5500629-5500836 | Common:3; Rare:79 | ||||
| chr17:5500960-5501123 | Common:2; Rare:60 | ||||
| chr17:5584429-5584599 | Common:2; Rare:36 | ||||
| chr17:5584767-5585086 | Common:8; Rare:55 |