| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1645702-1645855 | Common:2; Rare:44 | ||||
| chr17:1716185-1716544 | Common:3; Rare:112 | ||||
| chr17:1762689-1762805 | Common:2; Rare:30 | ||||
| chr17:1829805-1830063 | Common:7; Rare:109 | ||||
| chr17:2303450-2303656 | Rare:75 | ||||
| chr17:2303709-2303987 | Common:2; Rare:106 | ||||
| chr17:2336413-2336512 | Rare:41 | ||||
| chr17:2511806-2511954 | Common:2; Rare:44 | ||||
| chr17:2593486-2593688 | Common:3; Rare:73; Clinvar (benign):2 | ||||
| chr17:2593863-2593984 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711771-2712031 | Common:2; Rare:71 | ||||
| chr17:3636241-3636496 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr17:3636701-3636768 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr17:3668537-3668828 | Common:3; Rare:116 | ||||
| chr17:3723757-3723917 | Common:1; Rare:88 |