| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15860474-15860589 | Rare:32 | ||||
| chr10:16436777-16437022 | Common:2; Rare:54 | ||||
| chr10:16817364-16817734 | Common:4; Rare:132 | ||||
| chr10:17201612-17201769 | Common:2; Rare:55 | ||||
| chr10:17228463-17228715 | Common:1; Rare:68 | ||||
| chr10:17643871-17644253 | Common:2; Rare:116 | ||||
| chr10:18651564-18651693 | Common:1; Rare:51 | ||||
| chr10:21524536-21524663 | Rare:26 | ||||
| chr10:21533955-21534275 | Common:2; Rare:115 | ||||
| chr10:22316269-22316459 | Rare:83 | ||||
| chr10:24208760-24209184 | Common:1; Rare:120 | ||||
| chr10:26697570-26697768 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr10:27154315-27154483 | Rare:45 | ||||
| chr10:27155197-27155441 | Common:7; Rare:107; Clinvar:3; Clinvar (benign):7 | ||||
| chr10:27240714-27240877 | Rare:46 |