| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437292-39437456 | Common:2; Rare:59 | ||||
| chr2:40511774-40512005 | Common:1; Rare:41 | ||||
| chr2:42169148-42169429 | Common:1; Rare:138 | ||||
| chr2:43226598-43226865 | Common:2; Rare:105 | ||||
| chr2:43595908-43596222 | Common:1; Rare:110 | ||||
| chr2:43637094-43637330 | Common:2; Rare:79 | ||||
| chr2:43773951-43774140 | Common:5; Rare:79 | ||||
| chr2:43995802-43995832 | Rare:13; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:43995950-43996335 | Common:5; Rare:165; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44361479-44362062 | Common:4; Rare:187 | ||||
| chr2:46073688-46073873 | Rare:35 | ||||
| chr2:46297175-46297441 | Common:3; Rare:100 | ||||
| chr2:46541602-46541880 | Rare:64 | ||||
| chr2:46616978-46617263 | Common:7; Rare:124 | ||||
| chr2:46698944-46699334 | Common:1; Rare:120 |