| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2664167-2664265 | Common:2; Rare:43 | ||||
| chr20:2840672-2840771 | Common:1; Rare:46 | ||||
| chr20:2873396-2873711 | Common:3; Rare:99 | ||||
| chr20:3045894-3046098 | Common:1; Rare:57 | ||||
| chr20:3159811-3160048 | Rare:77 | ||||
| chr20:3173521-3173699 | Common:1; Rare:64 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3407514-3407755 | Common:3; Rare:68 | ||||
| chr20:3470915-3471039 | Common:1; Rare:48 | ||||
| chr20:3681976-3682334 | Common:4; Rare:93 | ||||
| chr20:3846724-3846893 | Rare:50 | ||||
| chr20:4148562-4148883 | Rare:90 | ||||
| chr20:4686209-4686508 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:5112815-5113168 | Common:2; Rare:124 | ||||
| chr20:5119906-5120174 | Common:1; Rare:90 |