| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49657303-49657660 | Common:4; Rare:122 | ||||
| chr22:50198171-50198421 | Common:1; Rare:107 | ||||
| chr22:50314490-50314593 | Common:1; Rare:48 | ||||
| chr3:4986833-4987077 | Common:1; Rare:55 | ||||
| chr3:9396205-9396322 | Rare:47 | ||||
| chr3:14810485-14810835 | Common:3; Rare:118 | ||||
| chr3:30608252-30608472 | Common:1; Rare:38 | ||||
| chr3:39411653-39412011 | Common:1; Rare:87; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:40453163-40453460 | Common:6; Rare:66 | ||||
| chr3:41225468-41225757 | Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:75434956-75435386 | Common:6; Rare:143 | ||||
| chr3:75672517-75672724 | Rare:1 | ||||
| chr3:101676241-101676478 | Common:2; Rare:78 | ||||
| chr3:104907521-104907761 | Common:6; Rare:87 | ||||
| chr3:107240636-107240755 | Rare:51 |