| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169566-42169618 | Common:2; Rare:28 | ||||
| chr2:43595957-43596207 | Common:1; Rare:90 | ||||
| chr2:43995943-43996335 | Common:5; Rare:169; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:44168115-44168238 | Common:1; Rare:40 | ||||
| chr2:44361408-44362115 | Common:4; Rare:240 | ||||
| chr2:44941434-44941778 | Rare:78 | ||||
| chr2:44941786-44941924 | Common:1; Rare:32 | ||||
| chr2:44942035-44942123 | Rare:37; Clinvar:1 | ||||
| chr2:46542254-46542342 | Common:1; Rare:16 | ||||
| chr2:46542407-46542636 | Rare:73 | ||||
| chr2:46615897-46616117 | Common:1; Rare:61 | ||||
| chr2:46616969-46617301 | Common:7; Rare:139; Clinvar (pathogenic):1 | ||||
| chr2:46698739-46698943 | Common:1; Rare:59 | ||||
| chr2:46699079-46699382 | Common:1; Rare:93 | ||||
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 |