| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36355544-36355948 | Common:4; Rare:250 | ||||
| chr2:36356007-36356393 | Common:6; Rare:190 | ||||
| chr2:36356332-36356732 | Common:2; Rare:222 | ||||
| chr2:36598141-36598289 | Common:30; Rare:120 | ||||
| chr2:36966504-36966936 | Common:9; Rare:314 | ||||
| chr2:37084264-37084561 | Common:7; Rare:207 | ||||
| chr2:37156905-37157169 | Common:5; Rare:129 | ||||
| chr2:37196396-37196546 | Common:1; Rare:97 | ||||
| chr2:37231539-37231767 | Common:9; Rare:244; Clinvar:2; Clinvar (benign):9 | ||||
| chr2:37324648-37324935 | Common:2; Rare:187 | ||||
| chr2:37924997-37925325 | Common:5; Rare:118 | ||||
| chr2:37925380-37925700 | Common:6; Rare:173 | ||||
| chr2:38076110-38076340 | Common:1; Rare:91 | ||||
| chr2:38076350-38076550 | Common:5; Rare:62 | ||||
| chr2:38076460-38077090 | Common:5; Rare:163 |