| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88691462-88691756 | Common:2; Rare:113; Clinvar:1 | ||||
| chr2:95165651-95165817 | Rare:49 | ||||
| chr2:95207434-95207538 | Rare:38 | ||||
| chr2:96208251-96208433 | Rare:89 | ||||
| chr2:96208787-96208956 | Common:3; Rare:69 | ||||
| chr2:96265951-96266344 | Common:2; Rare:119; Clinvar:2 | ||||
| chr2:96335707-96335812 | Common:1; Rare:34 | ||||
| chr2:96638292-96638511 | Common:1; Rare:56 | ||||
| chr2:97590296-97590603 | Common:1; Rare:56 | ||||
| chr2:97663897-97663987 | Common:1; Rare:35 | ||||
| chr2:98608423-98608659 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr2:99154899-99155031 | Common:1; Rare:51 | ||||
| chr2:99180971-99181238 | Common:2; Rare:77 | ||||
| chr2:100562626-100563046 | Common:5; Rare:122 | ||||
| chr2:101002164-101002313 | Rare:57 |