| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102066073-102066558 | Rare:382; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr10:102113477-102113877 | Common:3; Rare:80 | ||||
| chr10:102117194-102117733 | Common:1; Rare:137 | ||||
| chr10:102117857-102118071 | Common:2; Rare:82 | ||||
| chr10:102118904-102119131 | Common:2; Rare:76 | ||||
| chr10:102119622-102119923 | Common:2; Rare:106 | ||||
| chr10:102133545-102133753 | Common:1; Rare:50 | ||||
| chr10:102133678-102133810 | Rare:28 | ||||
| chr10:102133985-102134385 | Rare:171 | ||||
| chr10:102189542-102189647 | Rare:12 | ||||
| chr10:102246162-102246562 | Rare:64 | ||||
| chr10:102283557-102283957 | Common:4; Rare:165 | ||||
| chr10:102384672-102385417 | Common:2; Rare:188 | ||||
| chr10:102396308-102396708 | Common:6; Rare:122 | ||||
| chr10:102398629-102398814 | Rare:47; Clinvar:1 |