| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002221-176002420 | Common:3; Rare:86 | ||||
| chr2:176188538-176188668 | Common:1; Rare:50 | ||||
| chr2:177212586-177212810 | Common:1; Rare:94 | ||||
| chr2:177392672-177392853 | Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:177552770-177553068 | Common:4; Rare:86 | ||||
| chr2:178451090-178451310 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178651445-178651720 | Rare:90; Clinvar:9; Clinvar (benign):4 | ||||
| chr2:178807210-178807621 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:183037995-183038003 | |||||
| chr2:186486130-186486364 | Common:3; Rare:82 | ||||
| chr2:186589943-186590355 | Rare:125 | ||||
| chr2:189441131-189441501 | Common:2; Rare:107 | ||||
| chr2:189580753-189580938 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 | ||||
| chr2:189784276-189784512 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):1 |