| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3159781-3159954 | Rare:56 | ||||
| chr20:3173532-3173722 | Common:1; Rare:62 | ||||
| chr20:3204337-3204435 | Rare:40 | ||||
| chr20:3209133-3209343 | Common:1; Rare:41 | ||||
| chr20:3209424-3209549 | Common:1; Rare:45 | ||||
| chr20:3239557-3239734 | Common:1; Rare:51 | ||||
| chr20:3407950-3408024 | Rare:14 | ||||
| chr20:3470883-3471041 | Common:2; Rare:71 | ||||
| chr20:3767716-3767932 | Common:2; Rare:67 | ||||
| chr20:3795720-3795835 | Common:1; Rare:29 | ||||
| chr20:3796190-3796537 | Common:4; Rare:76 | ||||
| chr20:3820486-3820582 | Rare:39 | ||||
| chr20:3846718-3846892 | Rare:52 | ||||
| chr20:3888774-3888925 | Rare:36 | ||||
| chr20:3889157-3889396 | Common:1; Rare:124; Clinvar:5; Clinvar (benign):2 |