| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:195656662-195656931 | Rare:68 | ||||
| chr2:196926722-196926806 | Common:1; Rare:26 | ||||
| chr2:196927483-196927766 | Rare:59 | ||||
| chr2:197197651-197197986 | Common:3; Rare:49 | ||||
| chr2:197434970-197435186 | Rare:73 | ||||
| chr2:197453210-197453592 | Rare:140 | ||||
| chr2:197490195-197490517 | Common:2; Rare:65; Clinvar:1 | ||||
| chr2:197499788-197500439 | Common:2; Rare:248; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500649-197500820 | Rare:44 | ||||
| chr2:197515804-197516107 | Common:2; Rare:107 | ||||
| chr2:197675429-197675750 | Common:10; Rare:69 | ||||
| chr2:197675756-197675954 | Rare:37 | ||||
| chr2:197705081-197705430 | Common:3; Rare:156; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:199911136-199911438 | Rare:106 | ||||
| chr2:200306432-200306588 | Common:2; Rare:37 |