| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142877493-142877683 | Common:1; Rare:28 | ||||
| chr2:143128944-143129066 | Common:1; Rare:32 | ||||
| chr2:143129198-143129456 | Common:2; Rare:56 | ||||
| chr2:144331910-144332280 | Common:5; Rare:119 | ||||
| chr2:144332536-144332801 | Common:1; Rare:107 | ||||
| chr2:147844198-147844739 | Common:7; Rare:179 | ||||
| chr2:148020649-148021145 | Common:2; Rare:119; Clinvar (benign):2 | ||||
| chr2:148021409-148021541 | Rare:49 | ||||
| chr2:148644556-148644796 | Rare:78 | ||||
| chr2:148645137-148645462 | Rare:132 | ||||
| chr2:148875001-148875228 | Common:3; Rare:38 | ||||
| chr2:149587275-149587461 | Common:2; Rare:39 | ||||
| chr2:149587594-149587946 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:151261341-151261391 | Rare:19 | ||||
| chr2:151261395-151261589 | Common:4; Rare:70 |