| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58352088-58352315 | Common:5; Rare:165 | ||||
| chr17:58514514-58514763 | Rare:102 | ||||
| chr17:58517839-58518410 | Common:2; Rare:220 | ||||
| chr17:58692523-58692716 | Common:3; Rare:201; Clinvar:44; Clinvar (benign):42 | ||||
| chr17:59106592-59107297 | Common:7; Rare:303; Clinvar:11; Clinvar (benign):6 | ||||
| chr17:59154930-59155090 | Rare:77 | ||||
| chr17:59155128-59155345 | Common:2; Rare:112 | ||||
| chr17:59155546-59155796 | Rare:133 | ||||
| chr17:59209680-59210130 | Common:4; Rare:241 | ||||
| chr17:59220373-59220596 | Common:7; Rare:123 | ||||
| chr17:59565547-59565693 | Rare:119 | ||||
| chr17:59619160-59619420 | Common:4; Rare:98 | ||||
| chr17:59619492-59620113 | Common:6; Rare:379 | ||||
| chr17:59707368-59707748 | Common:4; Rare:104; Clinvar (benign):6 | ||||
| chr17:59837616-59838118 | Common:2; Rare:142 |