| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86366754-86366930 | Common:3; Rare:48 | ||||
| chr10:86521729-86521991 | Common:1; Rare:87 | ||||
| chr10:86756232-86756684 | Common:4; Rare:150 | ||||
| chr10:86756769-86757454 | Common:2; Rare:233; Clinvar (benign):6 | ||||
| chr10:86954456-86954649 | Common:3; Rare:43 | ||||
| chr10:87094817-87094932 | Rare:25; Clinvar:1 | ||||
| chr10:87095033-87095213 | Common:1; Rare:32 | ||||
| chr10:87504718-87504908 | Common:2; Rare:69 | ||||
| chr10:87660144-87660544 | Common:10; Rare:164 | ||||
| chr10:87818103-87818393 | Common:2; Rare:95 | ||||
| chr10:87863259-87863714 | Common:2; Rare:148; Clinvar:91; Clinvar (benign):9 | ||||
| chr10:87864237-87864706 | Common:2; Rare:207; Clinvar:40; Clinvar (benign):27; Clinvar (pathogenic):2 | ||||
| chr10:88880143-88880295 | Rare:40 | ||||
| chr10:88880490-88880930 | Common:5; Rare:106 | ||||
| chr10:88990689-88990873 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 |