| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519501-3519667 | Common:1; Rare:42 | ||||
| chr2:3558256-3558575 | Common:6; Rare:119 | ||||
| chr2:3575092-3575376 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:5692148-5692453 | Rare:71 | ||||
| chr2:6917278-6917500 | Rare:80 | ||||
| chr2:8681403-8682056 | Common:10; Rare:299 | ||||
| chr2:9003708-9004121 | Common:1; Rare:136 | ||||
| chr2:9206508-9206866 | Rare:126 | ||||
| chr2:9422575-9422862 | Common:1; Rare:44 | ||||
| chr2:9423463-9423698 | Rare:76 | ||||
| chr2:9555626-9556019 | Common:2; Rare:129 | ||||
| chr2:9630428-9630597 | Common:4; Rare:90 | ||||
| chr2:9630948-9631319 | Common:3; Rare:120 | ||||
| chr2:9843206-9843757 | Common:13; Rare:187 | ||||
| chr2:9951380-9951720 | Common:2; Rare:104 |