| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135985391-135985730 | Common:4; Rare:137; Clinvar (benign):1 | ||||
| chr2:138501645-138502011 | Common:4; Rare:135 | ||||
| chr2:144517332-144517732 | Common:5; Rare:123; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:148020681-148021112 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021544-148021658 | Rare:22 | ||||
| chr2:149330354-149330647 | Common:2; Rare:121 | ||||
| chr2:149587306-149587372 | Rare:13 | ||||
| chr2:149587674-149587823 | Common:1; Rare:41; Clinvar:1 | ||||
| chr2:151289609-151289704 | Common:1; Rare:26 | ||||
| chr2:151828459-151828627 | Common:2; Rare:46 | ||||
| chr2:152175888-152176163 | Common:1; Rare:69 | ||||
| chr2:152717829-152717964 | Rare:56 | ||||
| chr2:152717991-152718078 | Rare:26 | ||||
| chr2:152718485-152718654 | Rare:69 |