| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208258-96208457 | Rare:99 | ||||
| chr2:96208804-96208954 | Common:3; Rare:58 | ||||
| chr2:96260574-96260870 | Rare:41 | ||||
| chr2:96265479-96265612 | Rare:33 | ||||
| chr2:96265946-96266260 | Common:2; Rare:91; Clinvar:2 | ||||
| chr2:96305503-96305636 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:96536625-96536783 | Common:1; Rare:47 | ||||
| chr2:97646008-97646186 | Common:1; Rare:61 | ||||
| chr2:98608437-98608629 | Common:1; Rare:84 | ||||
| chr2:99154863-99155063 | Common:2; Rare:81; Clinvar (benign):2 | ||||
| chr2:99180985-99181227 | Common:2; Rare:71 | ||||
| chr2:100562693-100563069 | Common:4; Rare:120 | ||||
| chr2:101273025-101273192 | Rare:45 | ||||
| chr2:101991678-101991965 | Common:1; Rare:71 | ||||
| chr2:108534140-108534477 | Common:7; Rare:137 |