| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138501679-138502046 | Common:2; Rare:122 | ||||
| chr2:144517331-144517659 | Common:5; Rare:92; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144518397-144518498 | Rare:24 | ||||
| chr2:144520136-144520535 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:148020692-148021100 | Common:2; Rare:94; Clinvar (benign):2 | ||||
| chr2:149587706-149587816 | Common:1; Rare:30; Clinvar:1 | ||||
| chr2:151828482-151828793 | Common:2; Rare:84 | ||||
| chr2:152175670-152176052 | Common:2; Rare:108 | ||||
| chr2:152717824-152717964 | Rare:57 | ||||
| chr2:152717988-152718288 | Common:1; Rare:96 | ||||
| chr2:156332695-156332904 | Rare:62; Clinvar:2 | ||||
| chr2:159615469-159615731 | Common:2; Rare:84 | ||||
| chr2:159616411-159616612 | Common:2; Rare:42 | ||||
| chr2:159712372-159712593 | Common:2; Rare:88 | ||||
| chr2:159904698-159904905 | Rare:49 |