| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:23927065-23927308 | Common:3; Rare:88 | ||||
| chr2:24076284-24076594 | Rare:79 | ||||
| chr2:24123255-24123506 | Common:1; Rare:66 | ||||
| chr2:24971917-24972153 | Common:1; Rare:75 | ||||
| chr2:25878455-25878657 | Common:1; Rare:62 | ||||
| chr2:26244592-26244965 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345789-26346152 | Common:1; Rare:105 | ||||
| chr2:26764210-26764305 | Rare:31 | ||||
| chr2:27032872-27033000 | Rare:47 | ||||
| chr2:27212261-27212387 | Common:2; Rare:65 | ||||
| chr2:27323058-27323145 | Rare:23 | ||||
| chr2:27356750-27357080 | Rare:94 | ||||
| chr2:27370310-27370656 | Common:1; Rare:138 | ||||
| chr2:27628977-27629054 | Common:1; Rare:38 | ||||
| chr2:27663395-27663425 | Rare:7 |