| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37156921-37157242 | Common:7; Rare:98 | ||||
| chr2:37231559-37231696 | Common:4; Rare:75; Clinvar (benign):3 | ||||
| chr2:37671592-37671745 | Common:1; Rare:72 | ||||
| chr2:38076143-38076291 | Rare:38 | ||||
| chr2:38751348-38751625 | Common:4; Rare:126 | ||||
| chr2:38875897-38876064 | Common:1; Rare:59 | ||||
| chr2:39437103-39437453 | Common:4; Rare:122 | ||||
| chr2:39779213-39779362 | Common:4; Rare:50 | ||||
| chr2:42169187-42169436 | Common:1; Rare:126 | ||||
| chr2:43595986-43596205 | Common:1; Rare:75 | ||||
| chr2:44361483-44361977 | Common:3; Rare:158 | ||||
| chr2:46616984-46617261 | Common:6; Rare:120 | ||||
| chr2:46698944-46699319 | Common:1; Rare:119 | ||||
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916032-46916122 | Common:2; Rare:26 |