| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2664175-2664255 | Common:1; Rare:35 | ||||
| chr20:2840631-2840771 | Common:1; Rare:56 | ||||
| chr20:2873357-2873486 | Common:2; Rare:39 | ||||
| chr20:3046274-3046396 | Common:1; Rare:51 | ||||
| chr20:3173521-3173722 | Common:1; Rare:68 | ||||
| chr20:3209429-3209542 | Common:1; Rare:38 | ||||
| chr20:3407547-3407746 | Common:3; Rare:53 | ||||
| chr20:3407893-3408024 | Common:1; Rare:36 | ||||
| chr20:3681906-3682322 | Common:4; Rare:117 | ||||
| chr20:3767702-3767900 | Common:1; Rare:63 | ||||
| chr20:3795666-3795799 | Common:2; Rare:41 | ||||
| chr20:3889082-3889396 | Common:2; Rare:172; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:4823565-4823910 | Common:1; Rare:78 | ||||
| chr20:5112854-5113185 | Common:1; Rare:121 | ||||
| chr20:5119934-5120149 | Common:1; Rare:70 |