| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190879834-190880475 | Common:4; Rare:137 | ||||
| chr2:190880568-190880968 | Common:28; Rare:672 | ||||
| chr2:190880999-190882064 | Common:18; Rare:1274 | ||||
| chr2:191013810-191014481 | Common:14; Rare:595; Clinvar:11; Clinvar (benign):12 | ||||
| chr2:191020051-191020960 | Common:12; Rare:782 | ||||
| chr2:191021007-191021137 | Common:1; Rare:31 | ||||
| chr2:191021121-191021521 | Common:2; Rare:87 | ||||
| chr2:191033050-191033390 | Common:2; Rare:65 | ||||
| chr2:191041670-191042100 | Common:3; Rare:128 | ||||
| chr2:191677448-191678227 | Common:30; Rare:816 | ||||
| chr2:191678271-191679059 | Common:4; Rare:805 | ||||
| chr2:191679390-191679790 | Common:1; Rare:76 | ||||
| chr2:191846534-191847084 | Common:6; Rare:280 | ||||
| chr2:191847003-191847108 | Rare:21 | ||||
| chr2:191847029-191847519 | Rare:266 |