| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105233-131105367 | Common:1; Rare:64 | ||||
| chr2:131492754-131493097 | Common:8; Rare:103 | ||||
| chr2:134918597-134918879 | Common:1; Rare:119 | ||||
| chr2:135531167-135531521 | Common:1; Rare:76 | ||||
| chr2:138501664-138501938 | Common:2; Rare:103 | ||||
| chr2:148020673-148021116 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr2:149587685-149587830 | Common:1; Rare:42; Clinvar:1 | ||||
| chr2:150485382-150485509 | Rare:30 | ||||
| chr2:151828459-151828793 | Common:2; Rare:95 | ||||
| chr2:152175882-152176087 | Common:1; Rare:55 | ||||
| chr2:152717829-152717947 | Rare:47 | ||||
| chr2:152717970-152718085 | Rare:39 | ||||
| chr2:152718278-152718647 | Common:2; Rare:134 | ||||
| chr2:156332714-156332870 | Rare:48; Clinvar:2 | ||||
| chr2:156436290-156436450 | Common:1; Rare:48 |