| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75516366-75516619 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75516874-75516912 | Rare:13; Clinvar:1 | ||||
| chr17:75525417-75525800 | Common:4; Rare:112 | ||||
| chr17:75525938-75525996 | Rare:14 | ||||
| chr17:75621730-75621885 | Rare:26 | ||||
| chr17:75666951-75667445 | Common:7; Rare:144 | ||||
| chr17:75667502-75667567 | Rare:16 | ||||
| chr17:75667592-75667725 | Common:1; Rare:39 | ||||
| chr17:75667740-75667946 | Rare:40 | ||||
| chr17:75721135-75721615 | Common:4; Rare:138; Clinvar:3 | ||||
| chr17:75721616-75721843 | Common:1; Rare:42 | ||||
| chr17:75764658-75764814 | Common:1; Rare:43 | ||||
| chr17:75765067-75765228 | Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779276-75779647 | Common:1; Rare:185 | ||||
| chr17:75779684-75780162 | Common:2; Rare:185 |