| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181529-175181594 | Rare:20 | ||||
| chr2:175181620-175181751 | Common:4; Rare:59 | ||||
| chr2:175181756-175181777 | Rare:4 | ||||
| chr2:176002221-176002422 | Common:3; Rare:87 | ||||
| chr2:177212429-177212821 | Common:4; Rare:158 | ||||
| chr2:177263823-177263918 | Rare:21 | ||||
| chr2:177392665-177393066 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552865 | Common:1; Rare:34 | ||||
| chr2:177618702-177619047 | Common:7; Rare:101 | ||||
| chr2:178194367-178194658 | Common:2; Rare:84 | ||||
| chr2:178451077-178451363 | Common:6; Rare:84; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178651241-178651541 | Common:1; Rare:84; Clinvar:9; Clinvar (benign):7 | ||||
| chr2:182716359-182716421 | Rare:14 | ||||
| chr2:183124249-183124443 | Common:4; Rare:63 | ||||
| chr2:186485998-186486344 | Common:3; Rare:97 |