| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218271057-218271457 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218282141-218283070 | Common:7; Rare:249 | ||||
| chr2:218286720-218287020 | Common:2; Rare:81 | ||||
| chr2:218287056-218287480 | Common:6; Rare:207 | ||||
| chr2:218291623-218292777 | Common:8; Rare:388 | ||||
| chr2:218322504-218322856 | Common:2; Rare:66 | ||||
| chr2:218322911-218323386 | Common:21; Rare:437 | ||||
| chr2:218323359-218323671 | Common:1; Rare:77; Clinvar:1 | ||||
| chr2:218334815-218335215 | Common:2; Rare:92 | ||||
| chr2:218397680-218398060 | Common:7; Rare:176 | ||||
| chr2:218397979-218398248 | Common:4; Rare:175 | ||||
| chr2:218398482-218398857 | Common:11; Rare:256 | ||||
| chr2:218399462-218400236 | Common:3; Rare:806 | ||||
| chr2:218400223-218400654 | Common:30; Rare:426 | ||||
| chr2:218400912-218401154 | Common:13; Rare:130 |