| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134918588-134918908 | Common:1; Rare:135 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135741602-135741956 | Common:4; Rare:125 | ||||
| chr2:135985407-135985704 | Common:4; Rare:127; Clinvar (benign):1 | ||||
| chr2:136118139-136118328 | Rare:49 | ||||
| chr2:137964142-137964607 | Common:2; Rare:88 | ||||
| chr2:138501664-138502010 | Common:2; Rare:122 | ||||
| chr2:144332452-144332672 | Rare:89 | ||||
| chr2:144517460-144517768 | Common:5; Rare:84 | ||||
| chr2:144518422-144518594 | Rare:32 | ||||
| chr2:144520320-144520513 | Common:4; Rare:38; Clinvar (benign):1 | ||||
| chr2:148020674-148021109 | Common:2; Rare:100; Clinvar (benign):2 | ||||
| chr2:148021395-148021535 | Rare:51 | ||||
| chr2:148021552-148021674 | Rare:23 | ||||
| chr2:149587255-149587380 | Common:1; Rare:25 |