| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58007184-58007288 | Rare:49 | ||||
| chr17:58007604-58007684 | Rare:23 | ||||
| chr17:58219223-58219342 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58352125-58352481 | Common:6; Rare:136 | ||||
| chr17:58692555-58692668 | Common:1; Rare:63; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106685-59106970 | Common:2; Rare:95; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:59155122-59155552 | Common:2; Rare:105 | ||||
| chr17:59155563-59155671 | Rare:34 | ||||
| chr17:59331487-59331803 | Common:2; Rare:102 | ||||
| chr17:59619557-59620169 | Common:3; Rare:207 | ||||
| chr17:59683339-59683677 | Common:1; Rare:53 | ||||
| chr17:59707386-59707760 | Common:3; Rare:102; Clinvar (benign):4 | ||||
| chr17:59837484-59838002 | Common:1; Rare:75 | ||||
| chr17:59838423-59838768 | Rare:60 | ||||
| chr17:59892929-59893155 | Rare:65 |