| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178790-74179047 | Common:3; Rare:74 | ||||
| chr2:74421639-74421759 | Rare:39 | ||||
| chr2:74440419-74440664 | Rare:64 | ||||
| chr2:74454825-74455123 | Rare:80 | ||||
| chr2:74458146-74458509 | Common:1; Rare:112 | ||||
| chr2:74465360-74465446 | Rare:23 | ||||
| chr2:74482942-74483110 | Common:1; Rare:62 | ||||
| chr2:74483234-74483387 | Common:1; Rare:62 | ||||
| chr2:74503309-74503454 | Rare:36 | ||||
| chr2:74507351-74507535 | Rare:55 | ||||
| chr2:74507669-74507789 | Rare:25 | ||||
| chr2:74529653-74529970 | Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74555624-74555791 | Common:1; Rare:49 | ||||
| chr2:74654112-74654295 | Rare:48 | ||||
| chr2:74833804-74834166 | Common:1; Rare:108 |