| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100987090-100987584 | Common:1; Rare:179; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996971-100997182 | Common:2; Rare:57 | ||||
| chr10:100997543-100997764 | Common:1; Rare:41 | ||||
| chr10:100998181-100998381 | Rare:49 | ||||
| chr10:100999189-100999329 | Common:2; Rare:26 | ||||
| chr10:100999697-100999936 | Common:1; Rare:69 | ||||
| chr10:101031102-101031492 | Common:1; Rare:89 | ||||
| chr10:101588120-101588342 | Rare:95 | ||||
| chr10:101600940-101601286 | Common:2; Rare:75 | ||||
| chr10:101695064-101695387 | Common:1; Rare:75 | ||||
| chr10:101817955-101818249 | Common:1; Rare:99 | ||||
| chr10:101818267-101818762 | Common:1; Rare:134 | ||||
| chr10:102056073-102056368 | Common:1; Rare:69 | ||||
| chr10:102114954-102115048 | Common:1; Rare:35 | ||||
| chr10:102120436-102120649 | Common:1; Rare:78 |