| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43225879-43226051 | Common:1; Rare:62 | ||||
| chr2:43226586-43226850 | Common:1; Rare:105 | ||||
| chr2:43595926-43596191 | Common:1; Rare:88 | ||||
| chr2:43898950-43899606 | Common:1; Rare:194; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:44361436-44362012 | Common:4; Rare:189 | ||||
| chr2:46073431-46073503 | Rare:18 | ||||
| chr2:46297134-46297438 | Common:5; Rare:116 | ||||
| chr2:46541581-46541800 | Rare:51 | ||||
| chr2:46542270-46542738 | Common:1; Rare:136 | ||||
| chr2:46616974-46617292 | Common:7; Rare:136; Clinvar (pathogenic):1 | ||||
| chr2:46698787-46699006 | Common:1; Rare:69 | ||||
| chr2:46699458-46699689 | Common:2; Rare:78 | ||||
| chr2:46914064-46914248 | Common:1; Rare:34 | ||||
| chr2:46915709-46915908 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916001-46916256 | Common:2; Rare:74 |