| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8295352-8295532 | Common:1; Rare:48 | ||||
| chr17:8435666-8436039 | Common:5; Rare:145 | ||||
| chr17:8965648-8965802 | Common:1; Rare:39 | ||||
| chr17:10036510-10036714 | Common:1; Rare:41 | ||||
| chr17:10697417-10697654 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729749-10729822 | Rare:38 | ||||
| chr17:10729972-10730128 | Common:3; Rare:34 | ||||
| chr17:11997354-11997607 | Rare:96 | ||||
| chr17:12789389-12789549 | Rare:59 | ||||
| chr17:13017941-13018333 | Common:7; Rare:131; Clinvar (benign):2 | ||||
| chr17:14069347-14069648 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:15262443-15262738 | Rare:64 | ||||
| chr17:15999568-16000032 | Common:3; Rare:197; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039551-16039733 | Common:1; Rare:50 | ||||
| chr17:16039767-16040067 | Common:3; Rare:55 |