| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138501675-138501971 | Common:2; Rare:104 | ||||
| chr2:148020692-148021109 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr2:148021331-148021397 | Rare:12 | ||||
| chr2:149587685-149587849 | Common:1; Rare:46; Clinvar:1 | ||||
| chr2:151828416-151828793 | Common:2; Rare:109 | ||||
| chr2:152717829-152717964 | Rare:56 | ||||
| chr2:152717991-152718288 | Common:1; Rare:96 | ||||
| chr2:152718453-152718654 | Rare:77 | ||||
| chr2:156436088-156436444 | Common:3; Rare:101 | ||||
| chr2:158968475-158968646 | Rare:53 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 | ||||
| chr2:159616434-159616705 | Common:2; Rare:52 | ||||
| chr2:159711983-159712294 | Common:3; Rare:87 | ||||
| chr2:159712411-159712616 | Common:2; Rare:77 | ||||
| chr2:161308346-161308543 | Common:2; Rare:50 |