| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:166375771-166376116 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166494173-166494348 | Common:1; Rare:32 | ||||
| chr2:168456540-168456844 | Rare:96 | ||||
| chr2:169362504-169362703 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169479377-169479559 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr2:169573748-169573989 | Common:2; Rare:69 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584702-169584816 | Rare:30 | ||||
| chr2:169694333-169694598 | Common:5; Rare:92 | ||||
| chr2:169733756-169734083 | Common:2; Rare:94 | ||||
| chr2:169798745-169798973 | Rare:63 | ||||
| chr2:170816465-170816763 | Common:4; Rare:66; Clinvar:1 | ||||
| chr2:170817189-170817315 | Common:5; Rare:26 | ||||
| chr2:170817623-170817741 | Rare:28 | ||||
| chr2:170818159-170818430 | Common:1; Rare:56 |