| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25673490-25673801 | Common:1; Rare:115 | ||||
| chr2:25878429-25878815 | Common:5; Rare:108 | ||||
| chr2:25982160-25982330 | Rare:32 | ||||
| chr2:25982406-25982533 | Rare:34 | ||||
| chr2:26033673-26034182 | Common:4; Rare:184 | ||||
| chr2:26172865-26173146 | Rare:53 | ||||
| chr2:26244594-26244972 | Common:2; Rare:138; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26245025-26245142 | Rare:30 | ||||
| chr2:26345066-26345371 | Common:1; Rare:54 | ||||
| chr2:26345748-26346187 | Common:2; Rare:134 | ||||
| chr2:26401690-26402040 | Common:6; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:26692409-26692809 | Common:2; Rare:132 | ||||
| chr2:26764176-26764321 | Common:1; Rare:55 | ||||
| chr2:26785710-26786083 | Rare:98 | ||||
| chr2:26847242-26847642 | Common:5; Rare:104 |