| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177212422-177212832 | Common:4; Rare:162 | ||||
| chr2:177231896-177232124 | Common:2; Rare:59 | ||||
| chr2:177263436-177263703 | Common:1; Rare:62 | ||||
| chr2:177264618-177264883 | Common:2; Rare:82 | ||||
| chr2:177392666-177392780 | Rare:27; Clinvar:1 | ||||
| chr2:177552761-177553064 | Common:4; Rare:93 | ||||
| chr2:178072696-178072846 | Rare:41 | ||||
| chr2:178451077-178451363 | Common:6; Rare:84; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478522-178478659 | Common:1; Rare:43 | ||||
| chr2:179264502-179264861 | Common:4; Rare:133 | ||||
| chr2:181457239-181457528 | Common:2; Rare:107 | ||||
| chr2:181891665-181892030 | Common:4; Rare:149 | ||||
| chr2:186485988-186486344 | Common:3; Rare:98 | ||||
| chr2:186589943-186590034 | Rare:24 | ||||
| chr2:187448220-187448396 | Rare:29 |