| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63437317-63437729 | Common:2; Rare:243; Clinvar (pathogenic):2 | ||||
| chr17:63445633-63446578 | Common:5; Rare:628 | ||||
| chr17:63446595-63446995 | Common:8; Rare:137 | ||||
| chr17:63476773-63477230 | Common:9; Rare:393; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:63477303-63477495 | Common:1; Rare:73 | ||||
| chr17:63550070-63550678 | Common:18; Rare:695 | ||||
| chr17:63551009-63551409 | Common:8; Rare:66 | ||||
| chr17:63600211-63600611 | Common:1; Rare:55 | ||||
| chr17:63600639-63601039 | Rare:288; Clinvar:10 | ||||
| chr17:63621733-63622994 | Common:7; Rare:1009 | ||||
| chr17:63623079-63623479 | Common:3; Rare:88 | ||||
| chr17:63699889-63700360 | Common:3; Rare:290 | ||||
| chr17:63741331-63741459 | Rare:30 | ||||
| chr17:63741691-63742443 | Common:21; Rare:772 | ||||
| chr17:63772809-63773209 | Common:3; Rare:76 |