| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60421628-60421735 | Rare:28 | ||||
| chr17:60421797-60421922 | Common:1; Rare:20 | ||||
| chr17:60422107-60422158 | Rare:12 | ||||
| chr17:60525660-60525731 | Common:1; Rare:22 | ||||
| chr17:60525786-60526367 | Common:2; Rare:198 | ||||
| chr17:60599662-60599847 | Rare:40 | ||||
| chr17:60599885-60600430 | Common:4; Rare:192 | ||||
| chr17:60677282-60677505 | Common:1; Rare:48 | ||||
| chr17:60677633-60677972 | Common:1; Rare:94 | ||||
| chr17:60887462-60887559 | Rare:21 | ||||
| chr17:61452298-61452575 | Rare:67 | ||||
| chr17:61862984-61863136 | Rare:32 | ||||
| chr17:61863145-61863323 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:61863326-61863362 | Rare:5 | ||||
| chr17:61863402-61863778 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2 |