| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44811314-44811392 | Common:3; Rare:31 | ||||
| chr2:45311570-45311726 | Common:1; Rare:30 | ||||
| chr2:45323345-45323526 | Rare:37 | ||||
| chr2:46099323-46099426 | Rare:20 | ||||
| chr2:46376353-46376752 | Common:5; Rare:129; Clinvar:2; Clinvar (benign):6 | ||||
| chr2:46378605-46378701 | Rare:42 | ||||
| chr2:46382305-46382589 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:46391724-46391989 | Common:2; Rare:54 | ||||
| chr2:46394133-46394360 | Rare:50 | ||||
| chr2:46500215-46500332 | Common:2; Rare:29 | ||||
| chr2:46518954-46519058 | Rare:29 | ||||
| chr2:46592559-46592655 | Rare:32 | ||||
| chr2:47803152-47803461 | Common:2; Rare:108; Clinvar:12; Clinvar (benign):13 | ||||
| chr2:47804755-47805023 | Common:1; Rare:111; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):7 | ||||
| chr2:47906432-47906739 | Common:2; Rare:124 |