| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86959134-86959534 | Common:7; Rare:180 | ||||
| chr10:86968230-86968706 | Common:14; Rare:302 | ||||
| chr10:87019999-87020399 | Common:17; Rare:233 | ||||
| chr10:87094000-87094423 | Rare:323; Clinvar (benign):1 | ||||
| chr10:87094691-87095268 | Common:3; Rare:444; Clinvar:9 | ||||
| chr10:87095280-87095540 | Common:1; Rare:117 | ||||
| chr10:87095552-87095784 | Common:2; Rare:98 | ||||
| chr10:87504108-87504680 | Common:2; Rare:124 | ||||
| chr10:87504688-87505065 | Common:6; Rare:340; Clinvar (pathogenic):1 | ||||
| chr10:87659486-87660985 | Common:32; Rare:651 | ||||
| chr10:87818135-87818409 | Common:4; Rare:230 | ||||
| chr10:87862188-87862855 | Rare:454; Clinvar:2 | ||||
| chr10:87863215-87863774 | Common:5; Rare:442; Clinvar:271; Clinvar (benign):23 | ||||
| chr10:88582880-88583034 | Common:4; Rare:82 | ||||
| chr10:88583196-88583419 | Rare:94 |