| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58352125-58352450 | Common:5; Rare:131 | ||||
| chr17:58692361-58692714 | Common:2; Rare:147; Clinvar:21; Clinvar (benign):21 | ||||
| chr17:59106701-59106970 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59154982-59155033 | Rare:19 | ||||
| chr17:59155122-59155781 | Common:2; Rare:169 | ||||
| chr17:59565451-59565674 | Common:1; Rare:86 | ||||
| chr17:59619563-59620057 | Common:3; Rare:173 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59837581-59838000 | Rare:62 | ||||
| chr17:59892715-59893161 | Common:1; Rare:121 | ||||
| chr17:59964706-59965060 | Common:2; Rare:106 | ||||
| chr17:60078910-60078974 | Common:4; Rare:35 | ||||
| chr17:60525927-60526290 | Common:2; Rare:121 | ||||
| chr17:62423707-62423986 | Common:1; Rare:95 | ||||
| chr17:62477953-62478062 | Common:1; Rare:33 |