| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105211-131105378 | Common:2; Rare:126 | ||||
| chr2:131492378-131492545 | Common:6; Rare:67 | ||||
| chr2:131492610-131493143 | Common:16; Rare:263 | ||||
| chr2:132416270-132416858 | Common:4; Rare:275 | ||||
| chr2:134918185-134918295 | Common:2; Rare:30 | ||||
| chr2:134918616-134918879 | Common:2; Rare:207 | ||||
| chr2:134919130-134919690 | Common:9; Rare:222 | ||||
| chr2:135530699-135531080 | Common:6; Rare:114 | ||||
| chr2:135531156-135531610 | Common:2; Rare:165 | ||||
| chr2:135741536-135741951 | Common:5; Rare:139 | ||||
| chr2:135876343-135876664 | Common:2; Rare:175 | ||||
| chr2:135985004-135985219 | Common:2; Rare:89 | ||||
| chr2:135985403-135985788 | Common:9; Rare:265; Clinvar (benign):2 | ||||
| chr2:136118049-136118280 | Rare:133 | ||||
| chr2:137963800-137964580 | Common:11; Rare:186 |