| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437071-39437464 | Common:4; Rare:140 | ||||
| chr2:42792742-42793051 | Common:2; Rare:72 | ||||
| chr2:43226331-43226351 | Rare:9 | ||||
| chr2:43226539-43226875 | Common:3; Rare:141 | ||||
| chr2:43595957-43596191 | Common:1; Rare:80 | ||||
| chr2:43676427-43676489 | Rare:15 | ||||
| chr2:44361479-44362005 | Common:3; Rare:165 | ||||
| chr2:45651642-45651675 | Rare:4 | ||||
| chr2:46542271-46542328 | Common:1; Rare:10 | ||||
| chr2:46543138-46543157 | Rare:5 | ||||
| chr2:46543285-46543446 | Rare:37 | ||||
| chr2:46617012-46617275 | Common:7; Rare:115 | ||||
| chr2:46915714-46915869 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941715-46941992 | Common:4; Rare:81; Clinvar (benign):1 | ||||
| chr2:47402925-47403189 | Common:1; Rare:120; Clinvar:38; Clinvar (benign):26 |