| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105192-131105356 | Common:1; Rare:70 | ||||
| chr2:131492292-131492441 | Common:3; Rare:66 | ||||
| chr2:131492754-131492972 | Common:5; Rare:72 | ||||
| chr2:131493041-131493140 | Common:1; Rare:28 | ||||
| chr2:131527810-131528072 | Common:2; Rare:71 | ||||
| chr2:134120122-134120256 | Common:2; Rare:52 | ||||
| chr2:134918585-134918886 | Common:1; Rare:127 | ||||
| chr2:135052193-135052323 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr2:135530524-135530595 | Rare:14 | ||||
| chr2:135531158-135531609 | Common:1; Rare:101 | ||||
| chr2:135876371-135876657 | Common:1; Rare:77 | ||||
| chr2:135985404-135985685 | Common:4; Rare:125; Clinvar (benign):1 | ||||
| chr2:135985876-135985960 | Common:1; Rare:21 | ||||
| chr2:136118127-136118342 | Rare:56 | ||||
| chr2:136765308-136765591 | Common:5; Rare:84 |