| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38751354-38751643 | Common:4; Rare:129 | ||||
| chr2:38875936-38876043 | Rare:36 | ||||
| chr2:42169168-42169454 | Common:1; Rare:140 | ||||
| chr2:44361764-44361996 | Common:1; Rare:69 | ||||
| chr2:46617032-46617261 | Common:6; Rare:96 | ||||
| chr2:46915738-46915892 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:53786938-53787164 | Rare:94 | ||||
| chr2:54558234-54558422 | Common:2; Rare:64 | ||||
| chr2:55050494-55050784 | Common:3; Rare:89 | ||||
| chr2:55519452-55519747 | Common:1; Rare:79 | ||||
| chr2:58241316-58241431 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:63840822-63841137 | Common:1; Rare:87 | ||||
| chr2:64653903-64654071 | Common:1; Rare:57 | ||||
| chr2:65227582-65227909 | Rare:96 | ||||
| chr2:68157525-68157890 | Common:1; Rare:183 |