| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43676392-43676472 | Rare:19 | ||||
| chr2:43995954-43996289 | Common:5; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44361479-44362038 | Common:4; Rare:177 | ||||
| chr2:46297105-46297413 | Common:6; Rare:124 | ||||
| chr2:46541647-46541817 | Rare:40 | ||||
| chr2:46542978-46543188 | Common:1; Rare:56 | ||||
| chr2:46543285-46543530 | Rare:53 | ||||
| chr2:46544029-46544304 | Rare:75 | ||||
| chr2:46616982-46617275 | Common:7; Rare:128 | ||||
| chr2:46698772-46698947 | Common:1; Rare:52 | ||||
| chr2:46698949-46699280 | Rare:107 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916091-46916175 | Rare:30 | ||||
| chr2:47176439-47176869 | Common:4; Rare:192; Clinvar (benign):5 | ||||
| chr2:47345045-47345174 | Rare:34 |