| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127811153-127811264 | Rare:33 | ||||
| chr2:127858077-127858206 | Common:1; Rare:75 | ||||
| chr2:127885950-127885975 | Rare:3 | ||||
| chr2:130181538-130181770 | Common:3; Rare:105 | ||||
| chr2:130182091-130182558 | Common:3; Rare:176 | ||||
| chr2:130342127-130342242 | Rare:45 | ||||
| chr2:130342640-130342939 | Common:5; Rare:95 | ||||
| chr2:130355772-130356065 | Common:2; Rare:82 | ||||
| chr2:130372588-130372781 | Common:1; Rare:56 | ||||
| chr2:131492279-131492585 | Common:8; Rare:121 | ||||
| chr2:131493013-131493095 | Common:1; Rare:23 | ||||
| chr2:134918585-134918865 | Common:1; Rare:111 | ||||
| chr2:135531178-135531508 | Common:1; Rare:68 | ||||
| chr2:137964143-137964515 | Common:2; Rare:64 | ||||
| chr2:148020682-148021102 | Common:2; Rare:97; Clinvar (benign):2 |