| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34955725-34955928 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147076-35147381 | Common:2; Rare:113 | ||||
| chr20:35174917-35175065 | Common:3; Rare:58 | ||||
| chr20:35284545-35284863 | Common:2; Rare:83 | ||||
| chr20:35455028-35455334 | Common:1; Rare:98 | ||||
| chr20:35542331-35542570 | Rare:80 | ||||
| chr20:35556969-35557246 | Common:2; Rare:86 | ||||
| chr20:35699286-35699467 | Rare:64; Clinvar (benign):3 | ||||
| chr20:35741618-35741660 | Common:1; Rare:13 | ||||
| chr20:35742064-35742651 | Common:5; Rare:188 | ||||
| chr20:36541269-36541555 | Common:2; Rare:83 | ||||
| chr20:36573383-36573627 | Rare:101 | ||||
| chr20:36605537-36605842 | Common:2; Rare:116 | ||||
| chr20:36773706-36773908 | Common:2; Rare:60 | ||||
| chr20:37178817-37179243 | Common:1; Rare:123 |