| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38602886-38603195 | Common:4; Rare:120 | ||||
| chr2:38751296-38751440 | Common:2; Rare:85 | ||||
| chr2:38875897-38876059 | Common:1; Rare:57 | ||||
| chr2:39437087-39437456 | Common:4; Rare:132 | ||||
| chr2:42169224-42169436 | Common:1; Rare:112 | ||||
| chr2:43595924-43596205 | Common:1; Rare:98 | ||||
| chr2:43676422-43676471 | Rare:15 | ||||
| chr2:44361483-44362005 | Common:3; Rare:165 | ||||
| chr2:46073670-46073988 | Common:2; Rare:61 | ||||
| chr2:46616984-46617275 | Common:7; Rare:127 | ||||
| chr2:46698956-46699340 | Common:1; Rare:119 | ||||
| chr2:46914036-46914282 | Common:1; Rare:40 | ||||
| chr2:46915721-46915869 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916007-46916167 | Common:2; Rare:54 | ||||
| chr2:46941694-46941828 | Common:3; Rare:47; Clinvar (benign):1 |