| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7548943-7549249 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558029-7558325 | Common:2; Rare:62 | ||||
| chr17:7558640-7558783 | Rare:31 | ||||
| chr17:7558839-7559269 | Common:3; Rare:109; Clinvar:1 | ||||
| chr17:7561803-7562005 | Common:2; Rare:55 | ||||
| chr17:7562833-7563366 | Common:1; Rare:135 | ||||
| chr17:7579266-7579726 | Common:1; Rare:163 | ||||
| chr17:7579742-7579904 | Common:1; Rare:64 | ||||
| chr17:7580210-7580581 | Common:1; Rare:112 | ||||
| chr17:7583535-7583865 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584054-7584098 | Rare:13 | ||||
| chr17:7674927-7675230 | Rare:88; Clinvar:27; Clinvar (benign):23; Clinvar (pathogenic):18 | ||||
| chr17:7686418-7686677 | Rare:64 | ||||
| chr17:7687463-7687698 | Rare:49 | ||||
| chr17:7843643-7843778 | Rare:48 |