| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58219216-58219314 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58692549-58692733 | Common:1; Rare:98; Clinvar:26; Clinvar (benign):24 | ||||
| chr17:59106695-59107018 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:59155168-59155520 | Common:2; Rare:76 | ||||
| chr17:59565529-59565660 | Rare:57 | ||||
| chr17:59619563-59620081 | Common:3; Rare:179 | ||||
| chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
| chr17:59837664-59837975 | Rare:44 | ||||
| chr17:59892739-59893161 | Common:1; Rare:115 | ||||
| chr17:59964706-59965060 | Common:2; Rare:106 | ||||
| chr17:60078910-60078993 | Common:4; Rare:41 | ||||
| chr17:60525912-60526275 | Common:2; Rare:121 | ||||
| chr17:62628020-62628153 | Rare:22 | ||||
| chr17:63550190-63550539 | Common:2; Rare:80 | ||||
| chr17:63773479-63773858 | Common:2; Rare:124 |