| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58692387-58692678 | Common:2; Rare:126; Clinvar:15; Clinvar (benign):20 | ||||
| chr17:59106668-59107009 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:59155101-59155514 | Common:2; Rare:98 | ||||
| chr17:59155557-59155800 | Rare:66 | ||||
| chr17:59220404-59220711 | Common:3; Rare:90 | ||||
| chr17:59331445-59331803 | Common:2; Rare:118 | ||||
| chr17:59565451-59565716 | Common:1; Rare:101 | ||||
| chr17:59619181-59619318 | Rare:35 | ||||
| chr17:59619538-59620104 | Common:3; Rare:198 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59837618-59837993 | Rare:55 | ||||
| chr17:59892848-59893248 | Common:1; Rare:124 | ||||
| chr17:59964706-59965090 | Common:2; Rare:117 | ||||
| chr17:60078917-60079014 | Common:4; Rare:42 | ||||
| chr17:60525920-60526338 | Common:2; Rare:148 |