| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131093122-131093251 | Common:1; Rare:47 | ||||
| chr2:131093343-131093865 | Common:2; Rare:194 | ||||
| chr2:131104597-131104765 | Rare:32 | ||||
| chr2:131104888-131105439 | Common:5; Rare:179 | ||||
| chr2:131492130-131492217 | Common:2; Rare:31 | ||||
| chr2:131492381-131492605 | Common:6; Rare:79 | ||||
| chr2:131492676-131493155 | Common:10; Rare:141 | ||||
| chr2:131527757-131527849 | Common:2; Rare:22 | ||||
| chr2:134119768-134120011 | Common:2; Rare:73 | ||||
| chr2:134918086-134918948 | Common:7; Rare:317 | ||||
| chr2:135052160-135052365 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:135052518-135052884 | Common:1; Rare:75 | ||||
| chr2:135530471-135530666 | Rare:43 | ||||
| chr2:135530692-135531025 | Common:4; Rare:76 | ||||
| chr2:135531160-135531781 | Common:1; Rare:154 |