| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131492059-131492445 | Common:7; Rare:145 | ||||
| chr2:131492754-131492947 | Common:4; Rare:62 | ||||
| chr2:131493013-131493140 | Common:1; Rare:37 | ||||
| chr2:134918589-134918908 | Common:1; Rare:134 | ||||
| chr2:135052206-135052325 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr2:135530547-135530988 | Common:4; Rare:101 | ||||
| chr2:135531153-135531625 | Common:1; Rare:106 | ||||
| chr2:135741440-135741963 | Common:6; Rare:164 | ||||
| chr2:135876294-135876625 | Common:1; Rare:103 | ||||
| chr2:135985388-135985720 | Common:4; Rare:136; Clinvar (benign):1 | ||||
| chr2:135985876-135986076 | Common:1; Rare:42 | ||||
| chr2:137964085-137964504 | Common:2; Rare:65 | ||||
| chr2:138501638-138502095 | Common:4; Rare:167 | ||||
| chr2:142130889-142131046 | Rare:39 | ||||
| chr2:142131462-142131636 | Common:3; Rare:29 |