| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200526009-200526224 | Common:2; Rare:67 | ||||
| chr2:200811324-200811589 | Common:1; Rare:84 | ||||
| chr2:200811801-200811943 | Rare:54 | ||||
| chr2:200864228-200864252 | Rare:7 | ||||
| chr2:200864625-200864791 | Rare:66 | ||||
| chr2:200889045-200889479 | Common:3; Rare:138 | ||||
| chr2:200963628-200963859 | Common:1; Rare:58 | ||||
| chr2:201071633-201072047 | Rare:85 | ||||
| chr2:201451456-201451832 | Common:2; Rare:95 | ||||
| chr2:201642629-201642743 | Rare:54 | ||||
| chr2:201780884-201781241 | Common:3; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238478-202238625 | Rare:49; Clinvar:1 | ||||
| chr2:202634795-202634997 | Common:1; Rare:77 | ||||
| chr2:202911613-202912303 | Common:3; Rare:168 | ||||
| chr2:203014626-203014915 | Common:1; Rare:87 |