| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191246118-191246314 | Common:1; Rare:61 | ||||
| chr2:191677833-191678161 | Common:4; Rare:93 | ||||
| chr2:191846976-191847123 | Rare:29 | ||||
| chr2:196068808-196068909 | Common:1; Rare:24 | ||||
| chr2:196799613-196799777 | Common:1; Rare:48 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453247-197453554 | Rare:103 | ||||
| chr2:197499792-197500151 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500216-197500424 | Common:1; Rare:87 | ||||
| chr2:197705228-197705392 | Common:1; Rare:61 | ||||
| chr2:199911161-199911349 | Rare:57 | ||||
| chr2:200811437-200811572 | Common:1; Rare:47 | ||||
| chr2:200889018-200889424 | Common:2; Rare:132 | ||||
| chr2:201071620-201072041 | Rare:89 | ||||
| chr2:201115933-201116208 | Common:2; Rare:48 |