| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144517639-144518203 | Common:3; Rare:110 | ||||
| chr2:144518236-144518527 | Common:1; Rare:72 | ||||
| chr2:144519937-144520563 | Common:4; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144521070-144521302 | Rare:31 | ||||
| chr2:144524429-144524649 | Common:4; Rare:56 | ||||
| chr2:147844932-147845047 | Common:4; Rare:15 | ||||
| chr2:148020682-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021365-148021474 | Rare:21 | ||||
| chr2:148021571-148021658 | Rare:18 | ||||
| chr2:148875580-148875645 | Rare:22; Clinvar (benign):1 | ||||
| chr2:149587326-149587414 | Common:1; Rare:20 | ||||
| chr2:149587674-149587832 | Common:1; Rare:45; Clinvar:1 | ||||
| chr2:151828459-151828793 | Common:2; Rare:95 | ||||
| chr2:152098651-152098768 | Rare:37 | ||||
| chr2:152099031-152099344 | Common:2; Rare:103; Clinvar (benign):2 |