| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130756051-130756360 | Common:3; Rare:110 | ||||
| chr2:130836716-130836951 | Common:2; Rare:89 | ||||
| chr2:131105193-131105375 | Common:1; Rare:84 | ||||
| chr2:131492754-131493107 | Common:8; Rare:108 | ||||
| chr2:132257804-132257859 | Common:1; Rare:16 | ||||
| chr2:134918580-134918859 | Common:1; Rare:108 | ||||
| chr2:135052180-135052310 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr2:135531177-135531514 | Common:1; Rare:70 | ||||
| chr2:135741712-135741960 | Common:1; Rare:96 | ||||
| chr2:135985413-135985660 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr2:135985664-135985675 | Rare:3 | ||||
| chr2:136765280-136765606 | Common:9; Rare:96 | ||||
| chr2:137964388-137964570 | Rare:42 | ||||
| chr2:138501658-138501931 | Common:1; Rare:105 | ||||
| chr2:138780249-138780510 | Rare:79 |