| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144518134-144518233 | Common:1; Rare:25 | ||||
| chr2:144520136-144520563 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr2:144524440-144524651 | Common:4; Rare:55 | ||||
| chr2:148020681-148021106 | Common:2; Rare:98; Clinvar (benign):2 | ||||
| chr2:148021331-148021453 | Rare:22 | ||||
| chr2:148021539-148021631 | Rare:19 | ||||
| chr2:149330351-149330670 | Common:2; Rare:132 | ||||
| chr2:149587278-149587380 | Common:1; Rare:23 | ||||
| chr2:149587669-149587877 | Common:1; Rare:59; Clinvar:2 | ||||
| chr2:150485183-150485218 | Common:1; Rare:6 | ||||
| chr2:150485466-150485509 | Rare:9 | ||||
| chr2:150486694-150487018 | Common:1; Rare:64 | ||||
| chr2:150487187-150487272 | Rare:19 | ||||
| chr2:151289619-151289694 | Common:1; Rare:25 | ||||
| chr2:151828336-151828655 | Common:3; Rare:101 |