| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50189892-50190074 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58324393-58324544 | Rare:44 | ||||
| chr17:59838561-59838861 | Common:1; Rare:47 | ||||
| chr17:61398055-61398385 | Common:4; Rare:68 | ||||
| chr17:64145765-64145975 | Common:2; Rare:54 | ||||
| chr17:64385320-64385511 | Common:1; Rare:29 | ||||
| chr17:64837112-64837292 | Common:1; Rare:48 | ||||
| chr17:64975559-64975712 | Common:1; Rare:53 | ||||
| chr17:68523543-68523813 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:68529852-68529996 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:76557631-76557811 | Common:1; Rare:65 | ||||
| chr17:78416939-78417245 | Common:2; Rare:68 | ||||
| chr17:79026389-79026472 | Common:1; Rare:16 | ||||
| chr17:79031569-79031891 | Common:3; Rare:59 | ||||
| chr17:82441903-82442216 | Common:2; Rare:97 |