| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134918588-134918886 | Common:1; Rare:127 | ||||
| chr2:135531167-135531520 | Common:1; Rare:76 | ||||
| chr2:135876352-135876625 | Common:1; Rare:80 | ||||
| chr2:135985147-135985177 | Rare:9 | ||||
| chr2:135985404-135985740 | Common:4; Rare:141; Clinvar (benign):1 | ||||
| chr2:136118147-136118283 | Rare:39 | ||||
| chr2:137964053-137964624 | Common:5; Rare:105 | ||||
| chr2:138501645-138502037 | Common:4; Rare:144 | ||||
| chr2:142877452-142877694 | Common:1; Rare:38 | ||||
| chr2:144517287-144517579 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518141 | |||||
| chr2:144520136-144520525 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:148020649-148021128 | Common:2; Rare:111; Clinvar (benign):2 | ||||
| chr2:148021348-148021477 | Rare:24 | ||||
| chr2:148021571-148021658 | Rare:18 |