| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75034944-75035168 | Common:2; Rare:108 | ||||
| chr17:75035279-75035395 | Rare:35 | ||||
| chr17:75036722-75037020 | Common:1; Rare:54 | ||||
| chr17:75077497-75077766 | Common:2; Rare:71 | ||||
| chr17:75078570-75078990 | Common:2; Rare:85 | ||||
| chr17:75079634-75079814 | Common:2; Rare:41 | ||||
| chr17:75096224-75096406 | Rare:35 | ||||
| chr17:75124313-75124681 | Common:3; Rare:72 | ||||
| chr17:75204949-75205115 | Rare:37 | ||||
| chr17:75412669-75412830 | Common:2; Rare:35 | ||||
| chr17:75426415-75426626 | Rare:48 | ||||
| chr17:75430342-75430648 | Rare:62 | ||||
| chr17:75517615-75517737 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:75526413-75526523 | Rare:20 | ||||
| chr17:75549460-75549680 | Common:1; Rare:47 |