| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138780300-138780463 | Rare:43 | ||||
| chr2:148020692-148021096 | Common:2; Rare:94; Clinvar (benign):2 | ||||
| chr2:148021552-148021658 | Rare:21 | ||||
| chr2:149587289-149587365 | Common:1; Rare:18 | ||||
| chr2:149587662-149587826 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:151289619-151289705 | Common:1; Rare:27 | ||||
| chr2:152717829-152717972 | Rare:61 | ||||
| chr2:152717982-152718078 | Rare:31 | ||||
| chr2:156436279-156436485 | Common:3; Rare:59 | ||||
| chr2:159286631-159286912 | Common:5; Rare:109 | ||||
| chr2:159712372-159712600 | Common:2; Rare:90 | ||||
| chr2:161160209-161160468 | Common:2; Rare:73 | ||||
| chr2:161308311-161308566 | Common:2; Rare:67 | ||||
| chr2:162344318-162344394 | Rare:25 | ||||
| chr2:169584744-169584809 | Rare:15 |