| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100229505-100229762 | Common:2; Rare:80 | ||||
| chr10:100267522-100267868 | Common:4; Rare:110 | ||||
| chr10:100286193-100286287 | Rare:26 | ||||
| chr10:100286597-100286807 | Common:5; Rare:104 | ||||
| chr10:100346461-100346733 | Common:4; Rare:61 | ||||
| chr10:100346802-100347119 | Common:1; Rare:59 | ||||
| chr10:100347352-100347376 | Rare:6 | ||||
| chr10:100528598-100528902 | Rare:43 | ||||
| chr10:100529821-100530037 | Common:1; Rare:60 | ||||
| chr10:100535705-100536005 | Common:6; Rare:114 | ||||
| chr10:100912473-100912529 | Common:1; Rare:9 | ||||
| chr10:100912691-100913111 | Common:1; Rare:128 | ||||
| chr10:100913303-100913454 | Common:1; Rare:43 | ||||
| chr10:100969425-100969574 | Common:1; Rare:29 | ||||
| chr10:100987351-100987669 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):2 |