| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135985404-135985720 | Common:4; Rare:133; Clinvar (benign):1 | ||||
| chr2:137964098-137964506 | Common:2; Rare:66 | ||||
| chr2:138501614-138501856 | Common:3; Rare:109 | ||||
| chr2:144517284-144517774 | Common:6; Rare:145; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:148020652-148021122 | Common:2; Rare:109; Clinvar (benign):2 | ||||
| chr2:148021490-148021679 | Rare:46; Clinvar (benign):1 | ||||
| chr2:148021732-148021801 | Rare:10 | ||||
| chr2:149587299-149587380 | Rare:20 | ||||
| chr2:149587657-149587814 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150474802-150474979 | Rare:37 | ||||
| chr2:150474985-150475258 | Rare:39 | ||||
| chr2:150487045-150487369 | Common:6; Rare:70 | ||||
| chr2:151828261-151828619 | Common:3; Rare:106 | ||||
| chr2:152175604-152176063 | Common:2; Rare:138 | ||||
| chr2:152659187-152659281 | Common:1; Rare:33 |