| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87342273-87342425 | Common:3; Rare:51 | ||||
| chr10:87342579-87342907 | Common:1; Rare:88 | ||||
| chr10:87862259-87862575 | Rare:151; Clinvar:1 | ||||
| chr10:92240649-92240932 | Common:1; Rare:71 | ||||
| chr10:93432329-93432631 | Common:1; Rare:46 | ||||
| chr10:96089847-96089876 | Rare:4 | ||||
| chr10:96090194-96090334 | Common:1; Rare:59 | ||||
| chr10:97717063-97717350 | Common:1; Rare:41 | ||||
| chr10:100347942-100348001 | Rare:17 | ||||
| chr10:100373311-100373642 | Common:3; Rare:71 | ||||
| chr10:101311234-101311296 | Common:2; Rare:12 | ||||
| chr10:102109136-102109442 | Rare:82 | ||||
| chr10:102642058-102642339 | Common:1; Rare:73 | ||||
| chr10:103277751-103278276 | Common:2; Rare:151; Clinvar (pathogenic):1 | ||||
| chr10:111076213-111076406 | Common:1; Rare:36 |