| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135876277-135876676 | Common:1; Rare:114 | ||||
| chr2:135985062-135985250 | Common:1; Rare:53 | ||||
| chr2:135985325-135985805 | Common:6; Rare:186; Clinvar (benign):1 | ||||
| chr2:135985904-135986071 | Common:1; Rare:37 | ||||
| chr2:136118121-136118255 | Rare:39 | ||||
| chr2:137964041-137964447 | Common:5; Rare:58 | ||||
| chr2:137964450-137964493 | Rare:8 | ||||
| chr2:137964578-137964850 | Rare:67 | ||||
| chr2:138501443-138501453 | Rare:1 | ||||
| chr2:138501487-138501879 | Common:3; Rare:147 | ||||
| chr2:138501901-138502198 | Common:1; Rare:74 | ||||
| chr2:138502202-138502297 | Rare:25 | ||||
| chr2:144332110-144332367 | Common:2; Rare:104 | ||||
| chr2:144332413-144332801 | Common:1; Rare:148 | ||||
| chr2:147843809-147844043 | Common:1; Rare:54 |