| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42792543-42792794 | Common:3; Rare:69 | ||||
| chr2:43226254-43226420 | Rare:74 | ||||
| chr2:43226545-43226856 | Common:2; Rare:131 | ||||
| chr2:43595957-43596169 | Common:1; Rare:69 | ||||
| chr2:43637105-43637328 | Common:2; Rare:75 | ||||
| chr2:44361483-44362005 | Common:3; Rare:165 | ||||
| chr2:46297041-46297342 | Common:6; Rare:127 | ||||
| chr2:46429056-46429195 | Rare:53 | ||||
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46698967-46699334 | Common:1; Rare:116 | ||||
| chr2:46915721-46915906 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916104 | Common:2; Rare:30 | ||||
| chr2:47345053-47345148 | Rare:26 | ||||
| chr2:47369100-47369513 | Common:3; Rare:169; Clinvar:10; Clinvar (benign):4 | ||||
| chr2:47402991-47403180 | Common:1; Rare:85; Clinvar:28; Clinvar (benign):21 |