| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:86337599-86337847 | Rare:68 | ||||
| chr2:86440659-86440906 | Common:3; Rare:83 | ||||
| chr2:86440983-86441674 | Common:4; Rare:362 | ||||
| chr2:86441970-86442917 | Common:5; Rare:341 | ||||
| chr2:86562922-86563027 | Rare:39 | ||||
| chr2:86563346-86563566 | Common:2; Rare:81 | ||||
| chr2:86623245-86623395 | Common:1; Rare:38 | ||||
| chr2:86623802-86624002 | Common:1; Rare:92 | ||||
| chr2:86719781-86719961 | Rare:37 | ||||
| chr2:88055755-88055977 | Common:1; Rare:80 | ||||
| chr2:88627381-88627954 | Common:3; Rare:162; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:88691416-88691673 | Common:3; Rare:81 | ||||
| chr2:95025816-95026470 | Common:1; Rare:165 | ||||
| chr2:95121095-95121495 | Common:1; Rare:108 | ||||
| chr2:95121789-95122131 | Rare:112 |