| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100987205-100987604 | Common:1; Rare:145; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996973-100997132 | Common:1; Rare:42 | ||||
| chr10:101031102-101031292 | Common:1; Rare:43 | ||||
| chr10:101588139-101588348 | Rare:86; Clinvar:1 | ||||
| chr10:101818328-101818762 | Common:1; Rare:119 | ||||
| chr10:102056100-102056369 | Common:1; Rare:64 | ||||
| chr10:102152029-102152435 | Common:3; Rare:130 | ||||
| chr10:102245219-102245590 | Common:1; Rare:69 | ||||
| chr10:102394315-102394713 | Common:1; Rare:101 | ||||
| chr10:102395536-102395735 | Common:1; Rare:53 | ||||
| chr10:102420997-102421224 | Rare:96 | ||||
| chr10:102432546-102432828 | Common:2; Rare:81 | ||||
| chr10:102714197-102714627 | Common:2; Rare:142 | ||||
| chr10:102776004-102776279 | Common:1; Rare:45 | ||||
| chr10:102869445-102869551 | Common:5; Rare:23 |