| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106442-59106480 | Rare:13 | ||||
| chr17:59106704-59107097 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59154974-59155355 | Common:1; Rare:116 | ||||
| chr17:59155404-59155784 | Rare:96 | ||||
| chr17:59619538-59620188 | Common:3; Rare:222 | ||||
| chr17:59683430-59683983 | Rare:86 | ||||
| chr17:59707366-59707751 | Common:4; Rare:104; Clinvar (benign):6 | ||||
| chr17:59837584-59838165 | Common:4; Rare:96 | ||||
| chr17:59838174-59838442 | Rare:62 | ||||
| chr17:59892709-59893323 | Common:1; Rare:171 | ||||
| chr17:59964684-59964833 | Common:2; Rare:67 | ||||
| chr17:59965047-59965092 | Rare:16 | ||||
| chr17:60078866-60079007 | Common:4; Rare:64 | ||||
| chr17:60526160-60526382 | Rare:87 | ||||
| chr17:60599693-60599815 | Rare:20 |