| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130836751-130836901 | Common:1; Rare:54 | ||||
| chr2:131093374-131093530 | Common:1; Rare:70 | ||||
| chr2:131105226-131105367 | Common:1; Rare:66 | ||||
| chr2:131493050-131493086 | Common:1; Rare:8 | ||||
| chr2:132416661-132416842 | Common:1; Rare:53 | ||||
| chr2:134918634-134918857 | Common:1; Rare:92 | ||||
| chr2:135531195-135531502 | Common:1; Rare:53 | ||||
| chr2:135876377-135876633 | Common:1; Rare:72 | ||||
| chr2:148020675-148021005 | Common:2; Rare:71 | ||||
| chr2:151828469-151828795 | Common:2; Rare:91 | ||||
| chr2:152717829-152717958 | Rare:53 | ||||
| chr2:156332675-156332865 | Rare:58; Clinvar:3 | ||||
| chr2:158968512-158968678 | Rare:48 | ||||
| chr2:159712372-159712577 | Common:2; Rare:81 | ||||
| chr2:165794187-165794298 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):1 |