| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3846690-3846893 | Rare:60 | ||||
| chr20:3888517-3888830 | Common:1; Rare:69 | ||||
| chr20:3888833-3888868 | Rare:7 | ||||
| chr20:3889155-3889387 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4015481-4015710 | Common:4; Rare:81 | ||||
| chr20:4148586-4148880 | Rare:84 | ||||
| chr20:4686219-4686495 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr20:4823589-4823839 | Common:1; Rare:57 | ||||
| chr20:5112862-5113201 | Common:1; Rare:127 | ||||
| chr20:5119903-5120175 | Common:1; Rare:92 | ||||
| chr20:5126538-5127112 | Common:4; Rare:180 | ||||
| chr20:5610859-5611154 | Common:2; Rare:99 | ||||
| chr20:5750329-5750471 | Rare:32 | ||||
| chr20:5911348-5911621 | Common:2; Rare:73 | ||||
| chr20:5950326-5950689 | Common:8; Rare:110 |