| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99775934-99776135 | Rare:23 | ||||
| chr10:99779344-99779516 | Common:4; Rare:20 | ||||
| chr10:99780208-99780344 | Rare:31 | ||||
| chr10:99796913-99797144 | Common:1; Rare:52; Clinvar:3 | ||||
| chr10:100020271-100020559 | Common:1; Rare:44 | ||||
| chr10:100371331-100371480 | Rare:37 | ||||
| chr10:100372605-100372911 | Common:6; Rare:48 | ||||
| chr10:100373300-100373736 | Common:3; Rare:95 | ||||
| chr10:100373811-100373885 | Common:1; Rare:10 | ||||
| chr10:101031937-101032133 | Rare:52 | ||||
| chr10:101060691-101060782 | Rare:23 | ||||
| chr10:101060915-101061279 | Common:2; Rare:117 | ||||
| chr10:101694531-101694630 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:101730005-101730236 | Common:1; Rare:51 | ||||
| chr10:102399477-102399588 | Rare:41 |