| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:89701408-89701638 | Common:1; Rare:66 | ||||
| chr10:91410221-91410439 | Common:2; Rare:83 | ||||
| chr10:91632990-91633223 | Common:1; Rare:71 | ||||
| chr10:91923652-91923918 | Common:1; Rare:103 | ||||
| chr10:92574018-92574113 | Common:1; Rare:27 | ||||
| chr10:92593024-92593169 | Common:2; Rare:44 | ||||
| chr10:93482166-93482477 | Common:2; Rare:78 | ||||
| chr10:93702505-93702723 | Common:3; Rare:73 | ||||
| chr10:95290911-95291149 | Common:2; Rare:94 | ||||
| chr10:95561338-95561611 | Common:4; Rare:83 | ||||
| chr10:95656626-95656969 | Common:1; Rare:97; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:95693856-95694088 | Common:3; Rare:87; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907781-95907916 | Common:1; Rare:40 | ||||
| chr10:96129992-96130053 | Rare:19 | ||||
| chr10:97401292-97401489 | Common:1; Rare:67 |