| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42194404-42194594 | Rare:68 | ||||
| chr17:42276270-42276492 | Rare:160 | ||||
| chr17:42288440-42289080 | Common:12; Rare:200 | ||||
| chr17:42388368-42388909 | Common:2; Rare:284; Clinvar:6 | ||||
| chr17:42423103-42423465 | Common:2; Rare:178; Clinvar:4 | ||||
| chr17:42458710-42458954 | Common:4; Rare:161 | ||||
| chr17:42520008-42520546 | Common:3; Rare:188 | ||||
| chr17:42536123-42536275 | Common:2; Rare:100; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42563560-42563960 | Common:2; Rare:121 | ||||
| chr17:42566927-42567250 | Common:7; Rare:183 | ||||
| chr17:42577600-42577896 | Common:2; Rare:267 | ||||
| chr17:42609305-42609772 | Common:16; Rare:377; Clinvar (benign):4 | ||||
| chr17:42659213-42659387 | Rare:79 | ||||
| chr17:42675880-42676260 | Common:4; Rare:122 | ||||
| chr17:42682341-42682561 | Rare:67 |