| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:89414673-89414790 | Common:3; Rare:55 | ||||
| chr10:89701440-89701617 | Common:1; Rare:44 | ||||
| chr10:90871903-90871992 | Common:3; Rare:32 | ||||
| chr10:91162694-91163075 | Common:3; Rare:105 | ||||
| chr10:91410185-91410465 | Common:3; Rare:99 | ||||
| chr10:91633047-91633196 | Rare:49 | ||||
| chr10:91923720-91923813 | Rare:36 | ||||
| chr10:92290985-92291372 | Common:5; Rare:125 | ||||
| chr10:92574003-92574122 | Common:1; Rare:38 | ||||
| chr10:92592952-92593089 | Common:2; Rare:34 | ||||
| chr10:93482203-93482257 | Common:2; Rare:25 | ||||
| chr10:94402467-94402502 | Rare:11 | ||||
| chr10:95290856-95291175 | Common:2; Rare:125 | ||||
| chr10:95561358-95561545 | Common:3; Rare:49 | ||||
| chr10:95693858-95694150 | Common:5; Rare:102; Clinvar (benign):3; Clinvar (pathogenic):1 |