| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108449091-108449277 | Rare:76 | ||||
| chr2:108534186-108534477 | Common:7; Rare:117 | ||||
| chr2:108719344-108719635 | Common:3; Rare:131; Clinvar (benign):2 | ||||
| chr2:108719738-108719993 | Common:1; Rare:83 | ||||
| chr2:108786496-108786850 | Common:7; Rare:156 | ||||
| chr2:109613596-109613753 | Common:2; Rare:46 | ||||
| chr2:109613817-109614008 | Common:2; Rare:67 | ||||
| chr2:109614166-109614364 | Common:2; Rare:64 | ||||
| chr2:110677950-110678292 | Rare:120 | ||||
| chr2:110732405-110732573 | Rare:56 | ||||
| chr2:111122392-111122855 | Common:3; Rare:183 | ||||
| chr2:111123170-111123368 | Rare:71 | ||||
| chr2:111884076-111884276 | Common:1; Rare:59 | ||||
| chr2:111898267-111898738 | Common:3; Rare:115; Clinvar (benign):1 | ||||
| chr2:111898753-111898986 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 |