| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97445981-97446225 | Rare:63 | ||||
| chr10:97498694-97498993 | Common:2; Rare:86 | ||||
| chr10:98134536-98134688 | Common:1; Rare:54 | ||||
| chr10:98134836-98134893 | Rare:17 | ||||
| chr10:98446856-98446971 | Rare:29 | ||||
| chr10:99430579-99430930 | Common:4; Rare:81 | ||||
| chr10:99659264-99659536 | Common:1; Rare:67 | ||||
| chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185895-100186184 | Rare:108 | ||||
| chr10:100229553-100229689 | Rare:49 | ||||
| chr10:100286603-100286751 | Common:5; Rare:84 | ||||
| chr10:100346921-100347459 | Common:3; Rare:124 | ||||
| chr10:100529823-100530010 | Common:1; Rare:52 | ||||
| chr10:100912667-100913026 | Common:1; Rare:106 | ||||
| chr10:100987210-100987584 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):1 |