| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501757-47502015 | Common:1; Rare:89 | ||||
| chr20:47659401-47659499 | Rare:27 | ||||
| chr20:49046166-49046390 | Common:3; Rare:70 | ||||
| chr20:49188152-49188240 | Rare:20 | ||||
| chr20:49219282-49219487 | Rare:102 | ||||
| chr20:49278029-49278235 | Rare:54 | ||||
| chr20:49278371-49278669 | Common:8; Rare:95 | ||||
| chr20:49812731-49812925 | Common:2; Rare:52 | ||||
| chr20:49915471-49915548 | Rare:32 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50115899-50116135 | Common:3; Rare:58 | ||||
| chr20:50153633-50153893 | Common:2; Rare:102 | ||||
| chr20:50190544-50190833 | Rare:84 | ||||
| chr20:50510076-50510460 | Common:3; Rare:150 | ||||
| chr20:50958474-50958850 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):4 |