| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:84452086-84452291 | Common:1; Rare:39 | ||||
| chr10:86521743-86521968 | Rare:75 | ||||
| chr10:86756261-86756645 | Common:4; Rare:131 | ||||
| chr10:86958469-86958621 | Rare:39 | ||||
| chr10:86968207-86968571 | Common:5; Rare:87 | ||||
| chr10:87094369-87094395 | Rare:5; Clinvar (benign):1 | ||||
| chr10:87094549-87094733 | Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:87094939-87095235 | Common:1; Rare:74; Clinvar:2 | ||||
| chr10:87504771-87505116 | Common:2; Rare:169; Clinvar (pathogenic):1 | ||||
| chr10:87505353-87505423 | Rare:18 | ||||
| chr10:87659437-87659703 | Common:1; Rare:49 | ||||
| chr10:87818126-87818366 | Common:2; Rare:81 | ||||
| chr10:87841283-87841658 | Common:1; Rare:52 | ||||
| chr10:87863328-87863647 | Common:2; Rare:103; Clinvar:63; Clinvar (benign):7 | ||||
| chr10:87864132-87864466 | Common:1; Rare:115; Clinvar:14; Clinvar (benign):10 |