| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58219223-58219372 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58352131-58352495 | Common:6; Rare:138 | ||||
| chr17:58692358-58692668 | Common:2; Rare:129; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106707-59106999 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155153-59155692 | Common:2; Rare:135 | ||||
| chr17:59331453-59331778 | Common:2; Rare:106 | ||||
| chr17:59565483-59565660 | Common:1; Rare:71 | ||||
| chr17:59619563-59620064 | Common:3; Rare:176 | ||||
| chr17:59620098-59620134 | Rare:13 | ||||
| chr17:59707402-59707735 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr17:59892877-59893168 | Common:1; Rare:87 | ||||
| chr17:59964693-59965092 | Common:2; Rare:123 | ||||
| chr17:60078910-60078991 | Common:4; Rare:41 | ||||
| chr17:60392025-60392254 | Common:2; Rare:56 | ||||
| chr17:60422411-60422530 | Rare:21 |