| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52777296-52777730 | Rare:99 | ||||
| chr3:52777829-52778015 | Common:1; Rare:35 | ||||
| chr3:52778301-52778391 | Rare:31 | ||||
| chr3:52778393-52778647 | Common:2; Rare:73 | ||||
| chr3:52787973-52788332 | Common:1; Rare:118 | ||||
| chr3:52794593-52794910 | Common:1; Rare:96 | ||||
| chr3:52797930-52798094 | Rare:34 | ||||
| chr3:52800237-52800440 | Rare:34 | ||||
| chr3:52802332-52802806 | Common:3; Rare:145 | ||||
| chr3:52804362-52804756 | Common:3; Rare:74 | ||||
| chr3:52804889-52805014 | Common:2; Rare:16 | ||||
| chr3:52830536-52830859 | Common:5; Rare:80 | ||||
| chr3:52831035-52831186 | Common:3; Rare:44 | ||||
| chr3:52834839-52834986 | Common:1; Rare:35 | ||||
| chr3:53130405-53130561 | Common:1; Rare:50; Clinvar (benign):3 |