| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10729907-10730093 | Common:4; Rare:57 | ||||
| chr17:11997358-11997600 | Rare:92 | ||||
| chr17:13017960-13018036 | Common:2; Rare:37; Clinvar (benign):2 | ||||
| chr17:13018038-13018278 | Common:4; Rare:59 | ||||
| chr17:14069341-14069587 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:15260755-15260909 | Rare:62; Clinvar (benign):2 | ||||
| chr17:15262464-15262748 | Rare:63 | ||||
| chr17:15699510-15699774 | Common:3; Rare:70 | ||||
| chr17:15999572-16000168 | Common:4; Rare:246; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr17:16040439-16040730 | Common:2; Rare:53 | ||||
| chr17:16217102-16217238 | Rare:40; Clinvar:1 | ||||
| chr17:16415693-16415824 | Common:1; Rare:36 | ||||
| chr17:17237403-17237704 | Common:4; Rare:68 | ||||
| chr17:17281198-17281556 | Common:1; Rare:107 | ||||
| chr17:17496388-17496511 | Rare:29 |