| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42562796-42562935 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:42563041-42563272 | Rare:84 | ||||
| chr17:42566974-42567206 | Common:3; Rare:79 | ||||
| chr17:42577625-42577940 | Common:1; Rare:154 | ||||
| chr17:42609085-42609169 | Rare:35 | ||||
| chr17:42609270-42609800 | Common:9; Rare:214; Clinvar (benign):2 | ||||
| chr17:42659106-42659470 | Rare:102 | ||||
| chr17:42659501-42659569 | Rare:16 | ||||
| chr17:42676922-42677041 | Rare:36 | ||||
| chr17:42682417-42682592 | Rare:41 | ||||
| chr17:42744360-42744875 | Common:1; Rare:109 | ||||
| chr17:42744880-42745200 | Common:3; Rare:112 | ||||
| chr17:42773252-42773676 | Rare:117 | ||||
| chr17:42798528-42798769 | Rare:85 | ||||
| chr17:42823948-42824063 | Common:1; Rare:36 |