| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:132416200-132416860 | Common:3; Rare:177 | ||||
| chr2:132670195-132670482 | Common:1; Rare:65 | ||||
| chr2:132671494-132671637 | Common:2; Rare:38 | ||||
| chr2:133568400-133568740 | Common:1; Rare:54 | ||||
| chr2:134119767-134119968 | Common:2; Rare:58 | ||||
| chr2:134918183-134918310 | Common:2; Rare:34 | ||||
| chr2:134918375-134918910 | Common:3; Rare:220 | ||||
| chr2:135052153-135052331 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:135530502-135530611 | Rare:24 | ||||
| chr2:135530758-135530988 | Common:3; Rare:52 | ||||
| chr2:135531159-135531551 | Common:1; Rare:84 | ||||
| chr2:135531834-135531988 | Common:1; Rare:44 | ||||
| chr2:135741519-135741992 | Common:5; Rare:155 | ||||
| chr2:135876367-135876664 | Common:1; Rare:82 | ||||
| chr2:135985503-135985809 | Common:5; Rare:122; Clinvar (benign):1 |