| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135052167-135052306 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr2:135531167-135531514 | Common:1; Rare:74 | ||||
| chr2:137964100-137964515 | Common:2; Rare:70 | ||||
| chr2:138501664-138502017 | Common:2; Rare:126 | ||||
| chr2:144517497-144517767 | Common:5; Rare:70 | ||||
| chr2:148020673-148021119 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr2:148021544-148021661 | Rare:22 | ||||
| chr2:149587685-149587892 | Common:1; Rare:59; Clinvar:1 | ||||
| chr2:151289861-151290209 | Common:2; Rare:44 | ||||
| chr2:151828459-151828610 | Common:2; Rare:39 | ||||
| chr2:152175882-152176121 | Common:1; Rare:59 | ||||
| chr2:152717829-152718029 | Rare:81 | ||||
| chr2:152718377-152718643 | Common:2; Rare:95 | ||||
| chr2:156436290-156436469 | Common:1; Rare:50 | ||||
| chr2:158968485-158968673 | Rare:58 |