| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142877473-142877736 | Common:2; Rare:39 | ||||
| chr2:144517385-144517684 | Common:5; Rare:80; Clinvar (benign):2 | ||||
| chr2:144520136-144520528 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:148020688-148021109 | Common:2; Rare:97; Clinvar (benign):2 | ||||
| chr2:148021528-148021611 | Rare:13 | ||||
| chr2:149330414-149330652 | Common:2; Rare:91 | ||||
| chr2:149587299-149587365 | Rare:18 | ||||
| chr2:149587634-149587873 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:150486970-150487272 | Common:6; Rare:57 | ||||
| chr2:151289611-151289727 | Common:1; Rare:30 | ||||
| chr2:151410087-151410195 | Rare:32 | ||||
| chr2:151828345-151828793 | Common:3; Rare:139 | ||||
| chr2:152175694-152176057 | Common:1; Rare:100 | ||||
| chr2:152335362-152335616 | Rare:88 | ||||
| chr2:152717815-152718315 | Common:1; Rare:179 |