| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196068761-196068909 | Common:1; Rare:43 | ||||
| chr2:196171470-196171897 | Common:1; Rare:129 | ||||
| chr2:196639473-196639680 | Rare:52 | ||||
| chr2:196926656-196926828 | Common:2; Rare:80 | ||||
| chr2:197197786-197197988 | Common:3; Rare:28 | ||||
| chr2:197434970-197435232 | Rare:84 | ||||
| chr2:197453244-197453570 | Rare:111 | ||||
| chr2:197499783-197500032 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500052-197500738 | Common:1; Rare:234 | ||||
| chr2:197515839-197516107 | Common:2; Rare:97 | ||||
| chr2:197675546-197675797 | Common:10; Rare:48 | ||||
| chr2:197705150-197705424 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199851100-199851253 | Common:1; Rare:66 | ||||
| chr2:199910981-199911477 | Common:2; Rare:170 | ||||
| chr2:200509867-200510221 | Common:2; Rare:125 |