| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2652944-2653036 | Rare:35 | ||||
| chr20:2664184-2664265 | Common:2; Rare:35 | ||||
| chr20:2840637-2840768 | Common:1; Rare:52 | ||||
| chr20:2873357-2873481 | Common:2; Rare:38 | ||||
| chr20:3045881-3046118 | Common:2; Rare:67 | ||||
| chr20:3159811-3159875 | Rare:29 | ||||
| chr20:3159876-3159945 | Rare:16 | ||||
| chr20:3209429-3209530 | Common:1; Rare:32 | ||||
| chr20:3767736-3767959 | Common:2; Rare:71 | ||||
| chr20:3795723-3795835 | Common:1; Rare:27 | ||||
| chr20:3846724-3846886 | Rare:48 | ||||
| chr20:3889157-3889387 | Common:1; Rare:118; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4815127-4815229 | Common:1; Rare:25 | ||||
| chr20:4823587-4823709 | Rare:19 | ||||
| chr20:5119874-5120185 | Common:1; Rare:105 |