| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17591365-17591461 | Common:1; Rare:32 | ||||
| chr17:17591573-17591932 | Common:2; Rare:105 | ||||
| chr17:17823540-17823926 | Common:5; Rare:162 | ||||
| chr17:18039050-18039426 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18039564-18039692 | Rare:47 | ||||
| chr17:18087788-18088026 | Rare:62 | ||||
| chr17:18183007-18183111 | Rare:36 | ||||
| chr17:18183329-18183511 | Rare:44 | ||||
| chr17:18183713-18183925 | Rare:97 | ||||
| chr17:18184032-18184406 | Common:1; Rare:172 | ||||
| chr17:18184578-18184771 | Rare:44 | ||||
| chr17:18225374-18225656 | Common:3; Rare:89 | ||||
| chr17:18254596-18254823 | Rare:73 | ||||
| chr17:18260370-18260685 | Rare:87 | ||||
| chr17:18260802-18260911 | Common:1; Rare:34 |