| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181561-130181760 | Common:2; Rare:90 | ||||
| chr2:130342121-130342265 | Rare:61; Clinvar:1 | ||||
| chr2:130342642-130342948 | Common:5; Rare:100 | ||||
| chr2:130372591-130372717 | Rare:43 | ||||
| chr2:131105045-131105375 | Common:2; Rare:110 | ||||
| chr2:131493038-131493119 | Common:1; Rare:23 | ||||
| chr2:131529415-131529611 | Common:2; Rare:102 | ||||
| chr2:134918563-134918863 | Common:1; Rare:118 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135985415-135985705 | Common:4; Rare:127; Clinvar (benign):1 | ||||
| chr2:136118139-136118329 | Rare:50 | ||||
| chr2:138501645-138502054 | Common:4; Rare:148 | ||||
| chr2:142130700-142130873 | Common:2; Rare:71 | ||||
| chr2:148020688-148021109 | Common:2; Rare:97; Clinvar (benign):2 | ||||
| chr2:149587093-149587390 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 |