| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8176331-8176441 | Rare:37 | ||||
| chr17:8248042-8248181 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249212-8249325 | Common:1; Rare:32 | ||||
| chr17:8630860-8631155 | Common:3; Rare:97 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:11997436-11997590 | Rare:52 | ||||
| chr17:13018016-13018287 | Common:5; Rare:71 | ||||
| chr17:14069440-14069580 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300806-14301081 | Common:1; Rare:76 | ||||
| chr17:15262430-15262738 | Rare:68 | ||||
| chr17:15999598-15999999 | Common:3; Rare:181; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:17281183-17281399 | Rare:85 | ||||
| chr17:17591589-17591911 | Common:2; Rare:91 | ||||
| chr17:18087787-18087999 | Rare:58 | ||||
| chr17:18314925-18315354 | Common:1; Rare:124 |