| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135052218-135052323 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr2:135530558-135530813 | Common:1; Rare:55 | ||||
| chr2:135531167-135531514 | Common:1; Rare:74 | ||||
| chr2:135985398-135985730 | Common:4; Rare:136; Clinvar (benign):1 | ||||
| chr2:137964108-137964506 | Common:2; Rare:63 | ||||
| chr2:138501647-138502005 | Common:4; Rare:132 | ||||
| chr2:142130962-142131016 | Rare:17 | ||||
| chr2:142877446-142877724 | Common:2; Rare:44 | ||||
| chr2:144332452-144332670 | Rare:88 | ||||
| chr2:144513766-144513955 | Rare:53 | ||||
| chr2:144517317-144517742 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518392-144518542 | Rare:33 | ||||
| chr2:144519937-144520581 | Common:5; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144524417-144524603 | Common:4; Rare:54 |