| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1829816-1830077 | Common:7; Rare:112 | ||||
| chr17:2303773-2303980 | Common:2; Rare:76 | ||||
| chr17:2336430-2336543 | Rare:43 | ||||
| chr17:2511812-2512021 | Common:2; Rare:65 | ||||
| chr17:2593818-2593984 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3636241-3636459 | Common:4; Rare:61; Clinvar (benign):1 | ||||
| chr17:3668557-3668849 | Common:2; Rare:118 | ||||
| chr17:3723802-3723925 | Rare:68 | ||||
| chr17:4143605-4143735 | Common:4; Rare:76 | ||||
| chr17:4263948-4264072 | Rare:51 | ||||
| chr17:4555371-4555503 | Common:1; Rare:52 | ||||
| chr17:4704116-4704250 | Rare:74 | ||||
| chr17:4731296-4731473 | Common:2; Rare:52 | ||||
| chr17:4806996-4807210 | Common:4; Rare:67 | ||||
| chr17:4833251-4833420 | Rare:52 |