| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:1744412-1744553 | Common:1; Rare:50 | ||||
| chr2:3379646-3379728 | Common:1; Rare:26 | ||||
| chr2:3519497-3519636 | Common:2; Rare:41 | ||||
| chr2:3558251-3558691 | Common:6; Rare:162 | ||||
| chr2:3575228-3575373 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423148-9423268 | Common:1; Rare:25 | ||||
| chr2:9423391-9423682 | Rare:89 | ||||
| chr2:9474464-9474631 | Common:7; Rare:69 | ||||
| chr2:9555611-9555926 | Common:2; Rare:102 | ||||
| chr2:9843251-9843521 | Common:6; Rare:78 | ||||
| chr2:10302715-10302908 | Common:3; Rare:70 | ||||
| chr2:10448354-10448716 | Common:1; Rare:112 | ||||
| chr2:10689875-10690025 | Common:2; Rare:61 | ||||
| chr2:15561297-15561397 | Rare:43 | ||||
| chr2:17753739-17754195 | Common:5; Rare:141; Clinvar (benign):1 |