| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9422595-9422850 | Common:1; Rare:39 | ||||
| chr2:9423126-9423817 | Common:1; Rare:189 | ||||
| chr2:9474484-9474642 | Common:6; Rare:72 | ||||
| chr2:9555615-9556057 | Common:2; Rare:146 | ||||
| chr2:9630940-9631316 | Common:3; Rare:120 | ||||
| chr2:9843411-9843564 | Common:4; Rare:42 | ||||
| chr2:10122419-10122819 | Common:7; Rare:160 | ||||
| chr2:10448427-10448787 | Rare:115 | ||||
| chr2:10689892-10690025 | Common:2; Rare:51 | ||||
| chr2:10812678-10812975 | Common:3; Rare:115 | ||||
| chr2:11465821-11466202 | Common:4; Rare:129 | ||||
| chr2:11746499-11746655 | Common:1; Rare:47; Clinvar:2 | ||||
| chr2:12716631-12717017 | Common:3; Rare:120 | ||||
| chr2:15561294-15561519 | Rare:72 | ||||
| chr2:17753682-17754181 | Common:5; Rare:155; Clinvar (benign):1 |