| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135985494-135985666 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr2:135985844-135985938 | Common:1; Rare:17 | ||||
| chr2:136118139-136118348 | Rare:56 | ||||
| chr2:138501661-138501866 | Common:1; Rare:91 | ||||
| chr2:143129011-143129441 | Common:2; Rare:94 | ||||
| chr2:144332452-144332655 | Rare:81 | ||||
| chr2:148020681-148021005 | Common:2; Rare:70 | ||||
| chr2:149587326-149587347 | Rare:5 | ||||
| chr2:149587681-149587766 | Common:1; Rare:24; Clinvar:1 | ||||
| chr2:149587768-149587861 | Rare:21 | ||||
| chr2:151410090-151410171 | Rare:23 | ||||
| chr2:151828467-151828638 | Common:2; Rare:47 | ||||
| chr2:152175685-152176077 | Common:2; Rare:109 | ||||
| chr2:152717829-152717943 | Rare:47 | ||||
| chr2:152717965-152718029 | Rare:22 |