| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43225748-43226033 | Common:3; Rare:112 | ||||
| chr2:43226178-43226351 | Rare:74 | ||||
| chr2:43226399-43226431 | Common:1; Rare:7 | ||||
| chr2:43226589-43226869 | Common:2; Rare:111 | ||||
| chr2:43595924-43596222 | Common:1; Rare:104 | ||||
| chr2:44361433-44362115 | Common:4; Rare:233 | ||||
| chr2:46297249-46297437 | Common:3; Rare:66 | ||||
| chr2:46375472-46375760 | Common:2; Rare:72 | ||||
| chr2:46616978-46617275 | Common:7; Rare:129 | ||||
| chr2:46698944-46699387 | Common:1; Rare:135 | ||||
| chr2:46915709-46915939 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916032-46916191 | Common:2; Rare:48 | ||||
| chr2:46941703-46941787 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr2:47176199-47176353 | Common:2; Rare:57 | ||||
| chr2:47176417-47176565 | Rare:106; Clinvar (benign):5 |