| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:185782215-185782516 | Common:1; Rare:46 | ||||
| chr2:189004031-189004362 | Rare:99; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):20 | ||||
| chr2:189577337-189577399 | Rare:5 | ||||
| chr2:190488524-190488818 | Rare:67 | ||||
| chr2:190499722-190500220 | Common:3; Rare:120 | ||||
| chr2:190881984-190882023 | Common:1; Rare:6 | ||||
| chr2:191007412-191007658 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr2:191206931-191206997 | Rare:10 | ||||
| chr2:191846444-191846581 | Common:2; Rare:60 | ||||
| chr2:191846587-191846620 | Rare:9 | ||||
| chr2:196167209-196167241 | Rare:7 | ||||
| chr2:196211383-196211517 | Common:1; Rare:26 | ||||
| chr2:196259986-196260166 | Common:1; Rare:36 | ||||
| chr2:197267680-197267965 | Common:5; Rare:40 | ||||
| chr2:197280175-197280287 | Common:3; Rare:19 |