| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025258-240025432 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136256-240136334 | Rare:28 | ||||
| chr2:240560756-240560873 | Common:1; Rare:51 | ||||
| chr2:240998233-240998371 | Rare:27 | ||||
| chr2:241102276-241102380 | Common:2; Rare:37 | ||||
| chr2:241149450-241149638 | Common:2; Rare:58 | ||||
| chr2:241242574-241242878 | Common:2; Rare:71 | ||||
| chr2:241271936-241272081 | Common:1; Rare:35 | ||||
| chr2:241272769-241272912 | Rare:49 | ||||
| chr2:241315109-241315405 | Common:5; Rare:100 | ||||
| chr2:241315616-241315994 | Common:5; Rare:146 | ||||
| chr2:241508551-241508901 | Common:1; Rare:114 | ||||
| chr2:241637030-241637231 | Common:1; Rare:79 | ||||
| chr2:241637539-241637704 | Common:1; Rare:89 | ||||
| chr2:241686752-241687046 | Common:2; Rare:93 |