| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42423214-42423456 | Common:2; Rare:108; Clinvar:1 | ||||
| chr17:42458635-42458971 | Common:9; Rare:323 | ||||
| chr17:42520060-42520460 | Common:1; Rare:137 | ||||
| chr17:42536054-42536324 | Common:6; Rare:194; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr17:42536310-42536825 | Common:7; Rare:296; Clinvar:19; Clinvar (pathogenic):11 | ||||
| chr17:42561651-42562448 | Common:3; Rare:264; Clinvar (benign):1 | ||||
| chr17:42563604-42563841 | Common:1; Rare:42 | ||||
| chr17:42566897-42567251 | Common:10; Rare:254 | ||||
| chr17:42577627-42577963 | Common:3; Rare:385 | ||||
| chr17:42609303-42609835 | Common:25; Rare:575; Clinvar (benign):6 | ||||
| chr17:42659148-42659476 | Rare:171 | ||||
| chr17:42674146-42674257 | Rare:28 | ||||
| chr17:42675034-42675786 | Common:2; Rare:279 | ||||
| chr17:42675937-42676243 | Common:5; Rare:161 | ||||
| chr17:42676772-42677477 | Common:3; Rare:304 |