| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50731919-50732319 | Common:1; Rare:138 | ||||
| chr20:50931374-50931784 | Common:2; Rare:165 | ||||
| chr20:50958484-50958858 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:51023074-51023246 | Rare:58 | ||||
| chr20:51562835-51563077 | Common:1; Rare:40 | ||||
| chr20:51767765-51768390 | Common:6; Rare:243 | ||||
| chr20:51801599-51801747 | Common:2; Rare:30 | ||||
| chr20:51801779-51801973 | Common:2; Rare:41 | ||||
| chr20:51802515-51802801 | Common:2; Rare:43 | ||||
| chr20:52191215-52191359 | Common:2; Rare:28 | ||||
| chr20:52191467-52191589 | Rare:42 | ||||
| chr20:52191712-52191844 | Rare:30 | ||||
| chr20:52192321-52192609 | Common:1; Rare:53 | ||||
| chr20:52972055-52972358 | Common:2; Rare:71 | ||||
| chr20:53593388-53594572 | Common:11; Rare:659 |