| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97687223-97687526 | Common:5; Rare:96 | ||||
| chr10:97737031-97737208 | Rare:64 | ||||
| chr10:98134556-98134688 | Common:1; Rare:43 | ||||
| chr10:98268188-98268449 | Common:3; Rare:68 | ||||
| chr10:98446860-98446977 | Rare:31 | ||||
| chr10:99430586-99430959 | Common:4; Rare:93 | ||||
| chr10:99659239-99659529 | Common:1; Rare:74 | ||||
| chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185920-100186110 | Rare:76 | ||||
| chr10:100286603-100286763 | Common:5; Rare:90 | ||||
| chr10:100347058-100347543 | Common:5; Rare:124 | ||||
| chr10:100529831-100530010 | Common:1; Rare:48 | ||||
| chr10:100912660-100913050 | Common:1; Rare:114 | ||||
| chr10:100913328-100913464 | Rare:34 | ||||
| chr10:100987228-100987571 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 |