| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197407113-197407374 | Common:2; Rare:39 | ||||
| chr2:197489194-197489296 | Rare:29; Clinvar (benign):1 | ||||
| chr2:197492594-197492670 | Common:1; Rare:19 | ||||
| chr2:197492728-197492986 | Common:1; Rare:45 | ||||
| chr2:197493434-197493562 | Rare:39; Clinvar (benign):1 | ||||
| chr2:197550327-197550659 | Rare:58 | ||||
| chr2:197663807-197663843 | Rare:8 | ||||
| chr2:199459293-199459519 | Common:1; Rare:64 | ||||
| chr2:199935574-199935636 | Rare:6 | ||||
| chr2:199940379-199940604 | Rare:39 | ||||
| chr2:200395982-200396005 | Rare:3 | ||||
| chr2:200416292-200416421 | Rare:15 | ||||
| chr2:200419734-200419970 | Common:3; Rare:29 | ||||
| chr2:200786990-200787126 | Rare:28 | ||||
| chr2:200787478-200787672 | Rare:34 |