| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41689287-41689608 | Common:3; Rare:116 | ||||
| chr17:41812617-41812814 | Common:3; Rare:37; Clinvar:2 | ||||
| chr17:41812898-41813037 | Rare:40 | ||||
| chr17:41918988-41919326 | Common:3; Rare:105 | ||||
| chr17:41930488-41930645 | Rare:45 | ||||
| chr17:41966610-41966837 | Common:1; Rare:82 | ||||
| chr17:42016352-42016642 | Rare:48 | ||||
| chr17:42017120-42017216 | Rare:16 | ||||
| chr17:42017364-42017576 | Common:1; Rare:80 | ||||
| chr17:42017593-42017689 | Rare:25 | ||||
| chr17:42423093-42423398 | Common:1; Rare:81; Clinvar:2 | ||||
| chr17:42458719-42458960 | Common:3; Rare:88 | ||||
| chr17:42566888-42567149 | Common:3; Rare:91 | ||||
| chr17:42577671-42577869 | Common:1; Rare:102 | ||||
| chr17:42609333-42609782 | Common:8; Rare:178; Clinvar (benign):2 |