| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46082286-46082331 | Common:2; Rare:9 | ||||
| chr22:46497430-46497587 | Common:1; Rare:31 | ||||
| chr22:50202482-50202557 | Rare:18 | ||||
| chr3:4825975-4826124 | Rare:26 | ||||
| chr3:4982561-4982869 | Common:1; Rare:60 | ||||
| chr3:4985963-4985981 | Rare:3 | ||||
| chr3:8393983-8394006 | Rare:8 | ||||
| chr3:9381705-9381941 | Common:4; Rare:42 | ||||
| chr3:9453754-9454056 | Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9466313-9466386 | Rare:11 | ||||
| chr3:9918596-9918788 | Common:1; Rare:30 | ||||
| chr3:9960462-9960641 | Common:1; Rare:31 | ||||
| chr3:11519297-11519534 | Common:1; Rare:30 | ||||
| chr3:12584681-12584704 | Rare:8 | ||||
| chr3:12585156-12585320 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):4 |