| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217978798-217978973 | Common:1; Rare:53 | ||||
| chr2:218217058-218217226 | Common:1; Rare:62 | ||||
| chr2:218270104-218270534 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218322988-218323275 | Common:6; Rare:93 | ||||
| chr2:218568301-218568957 | Common:5; Rare:173 | ||||
| chr2:218659605-218659738 | Rare:32 | ||||
| chr2:218671974-218672339 | Common:2; Rare:90 | ||||
| chr2:219176926-219177109 | Common:4; Rare:57 | ||||
| chr2:219178136-219178355 | Common:6; Rare:113 | ||||
| chr2:219206665-219206879 | Rare:84 | ||||
| chr2:219229582-219229875 | Common:2; Rare:78 | ||||
| chr2:219245416-219245531 | Rare:33 | ||||
| chr2:219253894-219254073 | Common:2; Rare:58 | ||||
| chr2:219279211-219279527 | Common:2; Rare:100 | ||||
| chr2:219419845-219420093 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 |