| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135769682-135769832 | Rare:31 | ||||
| chr2:135774871-135775215 | Common:2; Rare:57 | ||||
| chr2:135782133-135782168 | Rare:5 | ||||
| chr2:135932830-135932860 | Common:3; Rare:10; Clinvar (benign):2 | ||||
| chr2:135964581-135964768 | Common:1; Rare:33 | ||||
| chr2:136236803-136236996 | Common:5; Rare:27 | ||||
| chr2:136238804-136239147 | Common:1; Rare:63 | ||||
| chr2:136239152-136239286 | Common:1; Rare:24 | ||||
| chr2:137932654-137932804 | Common:1; Rare:24 | ||||
| chr2:137976035-137976037 | |||||
| chr2:138502625-138502738 | Rare:23 | ||||
| chr2:138505537-138505584 | Rare:9 | ||||
| chr2:138513588-138513941 | Common:2; Rare:72 | ||||
| chr2:138567351-138567458 | Rare:24 | ||||
| chr2:138567509-138567759 | Rare:37 |