| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:63588593-63589146 | Common:1; Rare:177; Clinvar (benign):1 | ||||
| chr2:63840734-63841180 | Common:3; Rare:136 | ||||
| chr2:63841319-63841920 | Common:2; Rare:173 | ||||
| chr2:64018796-64019040 | Rare:51 | ||||
| chr2:64019164-64019296 | Rare:32 | ||||
| chr2:64019310-64019640 | Rare:108 | ||||
| chr2:64144246-64144692 | Common:4; Rare:124 | ||||
| chr2:64453963-64454244 | Rare:55 | ||||
| chr2:64454289-64454489 | Rare:72 | ||||
| chr2:64454840-64454968 | Rare:30 | ||||
| chr2:64524055-64524611 | Common:3; Rare:172 | ||||
| chr2:64524973-64525033 | Rare:12 | ||||
| chr2:64653751-64654130 | Common:2; Rare:140 | ||||
| chr2:64750746-64751266 | Common:5; Rare:152 | ||||
| chr2:64988418-64988580 | Rare:31 |