| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100347168-100347268 | Common:1; Rare:24 | ||||
| chr10:100347309-100347510 | Common:3; Rare:49 | ||||
| chr10:100529812-100529992 | Common:1; Rare:55 | ||||
| chr10:100912642-100912993 | Common:1; Rare:103 | ||||
| chr10:100913334-100913464 | Rare:32 | ||||
| chr10:100987145-100987954 | Common:2; Rare:229; Clinvar:3; Clinvar (benign):4 | ||||
| chr10:100999637-100999872 | Common:1; Rare:70 | ||||
| chr10:101031093-101031500 | Common:1; Rare:94 | ||||
| chr10:101354015-101354233 | Common:1; Rare:85 | ||||
| chr10:101588081-101588360 | Rare:119; Clinvar:1 | ||||
| chr10:101694751-101695056 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:101695111-101695201 | Rare:23 | ||||
| chr10:101783367-101783482 | Rare:51 | ||||
| chr10:101817825-101818085 | Common:3; Rare:86 | ||||
| chr10:101818088-101818321 | Rare:75 |