| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131492953-131493106 | Common:4; Rare:42 | ||||
| chr2:134918589-134918886 | Common:1; Rare:126 | ||||
| chr2:135531164-135531606 | Common:1; Rare:99 | ||||
| chr2:135876343-135876641 | Common:1; Rare:89 | ||||
| chr2:138501675-138501946 | Common:2; Rare:97 | ||||
| chr2:148020678-148021105 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021522-148021679 | Rare:32; Clinvar (benign):1 | ||||
| chr2:149587326-149587418 | Common:1; Rare:22 | ||||
| chr2:149587659-149587823 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:152175638-152176015 | Common:2; Rare:106 | ||||
| chr2:152717845-152718055 | Rare:80 | ||||
| chr2:152718494-152718662 | Rare:68 | ||||
| chr2:157257836-157258018 | Common:1; Rare:23 | ||||
| chr2:157875791-157875885 | Rare:25 | ||||
| chr2:158456685-158456952 | Common:1; Rare:91 |