| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42185630-42186020 | Common:3; Rare:80 | ||||
| chr17:42194448-42194620 | Rare:29 | ||||
| chr17:42276340-42276710 | Common:1; Rare:196 | ||||
| chr17:42388354-42388474 | Rare:38; Clinvar:3 | ||||
| chr17:42423229-42423514 | Common:1; Rare:76; Clinvar:1 | ||||
| chr17:42458710-42458942 | Common:3; Rare:86 | ||||
| chr17:42536118-42536273 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:42561983-42562193 | Common:1; Rare:68 | ||||
| chr17:42566939-42567123 | Common:3; Rare:63 | ||||
| chr17:42577667-42577924 | Common:1; Rare:130 | ||||
| chr17:42609322-42609772 | Common:8; Rare:186; Clinvar (benign):2 | ||||
| chr17:42659171-42659302 | Rare:39 | ||||
| chr17:42682420-42682632 | Common:1; Rare:50 | ||||
| chr17:42709420-42709780 | Rare:57 | ||||
| chr17:42744633-42744797 | Rare:36 |