| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135530664-135531025 | Common:4; Rare:82 | ||||
| chr2:135531152-135531570 | Common:1; Rare:93 | ||||
| chr2:135531839-135531948 | Common:1; Rare:31 | ||||
| chr2:135741525-135741963 | Common:5; Rare:145 | ||||
| chr2:135741996-135742254 | Rare:77 | ||||
| chr2:135742631-135742695 | Rare:16 | ||||
| chr2:135875609-135876013 | Common:2; Rare:99 | ||||
| chr2:135876315-135876663 | Common:1; Rare:105 | ||||
| chr2:135984750-135985285 | Common:1; Rare:124 | ||||
| chr2:135985440-135985675 | Common:4; Rare:106; Clinvar (benign):1 | ||||
| chr2:136116514-136116597 | Common:2; Rare:14 | ||||
| chr2:136117161-136117436 | Common:2; Rare:73 | ||||
| chr2:136118002-136118314 | Rare:82 | ||||
| chr2:138501482-138501994 | Common:4; Rare:179 | ||||
| chr2:138502071-138502235 | Rare:42 |