| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484690-7484795 | Rare:47 | ||||
| chr17:7548924-7549243 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558388-7558783 | Rare:81 | ||||
| chr17:7561784-7562008 | Common:2; Rare:61 | ||||
| chr17:7579198-7579524 | Common:1; Rare:123 | ||||
| chr17:7580143-7580585 | Common:1; Rare:130 | ||||
| chr17:7580772-7581060 | Common:1; Rare:76 | ||||
| chr17:7583508-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584069-7584288 | Common:1; Rare:50 | ||||
| chr17:7627585-7627593 | Rare:1 | ||||
| chr17:7674911-7675219 | Rare:91; Clinvar:28; Clinvar (benign):24; Clinvar (pathogenic):18 | ||||
| chr17:7686413-7686692 | Rare:69 | ||||
| chr17:7687469-7687681 | Rare:45 | ||||
| chr17:7843643-7843762 | Rare:41 | ||||
| chr17:7843935-7844519 | Common:8; Rare:161 |