| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195895751-195897180 | Common:20; Rare:1304 | ||||
| chr3:195909350-195910160 | Common:30; Rare:775 | ||||
| chr3:195911860-195912300 | Common:4; Rare:91 | ||||
| chr3:196081397-196081821 | Common:4; Rare:198 | ||||
| chr3:196081855-196082317 | Common:13; Rare:572 | ||||
| chr3:196270404-196270851 | Common:4; Rare:167; Clinvar (pathogenic):2 | ||||
| chr3:196287120-196287559 | Common:3; Rare:158 | ||||
| chr3:196287519-196288200 | Common:10; Rare:783 | ||||
| chr3:196288361-196288550 | Common:1; Rare:47 | ||||
| chr3:196317780-196318459 | Common:18; Rare:1044; Clinvar (pathogenic):4 | ||||
| chr3:196337502-196338090 | Common:3; Rare:188 | ||||
| chr3:196338334-196338880 | Common:2; Rare:352 | ||||
| chr3:196431809-196432705 | Common:8; Rare:810 | ||||
| chr3:196503293-196503990 | Common:32; Rare:612 | ||||
| chr3:196568396-196569288 | Common:35; Rare:675 |