| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48578380-48578425 | Common:1; Rare:12 | ||||
| chr17:49691171-49691334 | Common:2; Rare:29 | ||||
| chr17:50189876-50190074 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:58324380-58324544 | Rare:47 | ||||
| chr17:59829257-59829547 | Common:1; Rare:39 | ||||
| chr17:59830347-59830366 | Rare:4 | ||||
| chr17:59851724-59851899 | Common:1; Rare:26 | ||||
| chr17:64145750-64145975 | Common:2; Rare:59 | ||||
| chr17:64355024-64355225 | Rare:24 | ||||
| chr17:64837112-64837310 | Common:1; Rare:56 | ||||
| chr17:64975045-64975326 | Common:2; Rare:56 | ||||
| chr17:64975362-64975727 | Common:3; Rare:115 | ||||
| chr17:65100701-65100911 | Rare:65 | ||||
| chr17:68101486-68101572 | Common:3; Rare:43 | ||||
| chr17:75722202-75722279 | Rare:10 |