| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45934541-45934698 | Common:1; Rare:79 | ||||
| chr20:46364381-46364522 | Rare:52 | ||||
| chr20:47356711-47356853 | Rare:32 | ||||
| chr20:47501764-47501925 | Common:1; Rare:57 | ||||
| chr20:49278048-49278278 | Rare:65 | ||||
| chr20:50113124-50113235 | Common:5; Rare:52 | ||||
| chr20:50958482-50958834 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:51802449-51802727 | Common:1; Rare:52 | ||||
| chr20:56392169-56392397 | Rare:61 | ||||
| chr20:58651144-58651284 | Common:2; Rare:27; Clinvar (benign):1 | ||||
| chr20:62143304-62143739 | Common:5; Rare:184 | ||||
| chr20:62182915-62183042 | Rare:45 | ||||
| chr20:62386946-62387126 | Common:3; Rare:80 | ||||
| chr20:62926476-62926625 | Common:2; Rare:52 | ||||
| chr20:62937883-62938209 | Common:2; Rare:117 |