| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206085824-206085986 | Common:1; Rare:44 | ||||
| chr2:206159192-206159238 | Common:2; Rare:12 | ||||
| chr2:206159340-206159919 | Common:4; Rare:153; Clinvar (benign):1 | ||||
| chr2:206161820-206162105 | Rare:88 | ||||
| chr2:206162573-206162874 | Common:1; Rare:74 | ||||
| chr2:206274505-206274722 | Rare:57 | ||||
| chr2:206765276-206765680 | Common:3; Rare:111; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:207134374-207134468 | Common:2; Rare:20 | ||||
| chr2:207165762-207166115 | Rare:68 | ||||
| chr2:207166816-207167002 | Common:3; Rare:79 | ||||
| chr2:207529960-207530131 | Rare:44 | ||||
| chr2:207624569-207624692 | Rare:29 | ||||
| chr2:208025493-208025618 | Rare:34 | ||||
| chr2:208255018-208255228 | Common:2; Rare:55 | ||||
| chr2:208266121-208266409 | Common:6; Rare:98; Clinvar:1; Clinvar (benign):2 |