| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:348143-348306 | Common:1; Rare:41 | ||||
| chr20:1118458-1118683 | Common:3; Rare:71 | ||||
| chr20:1894178-1894487 | Common:3; Rare:72 | ||||
| chr20:2508876-2509225 | Common:1; Rare:73 | ||||
| chr20:2652430-2652658 | Common:8; Rare:79 | ||||
| chr20:2664181-2664284 | Common:3; Rare:44 | ||||
| chr20:2840631-2840764 | Common:1; Rare:52 | ||||
| chr20:3159826-3160012 | Rare:61 | ||||
| chr20:3209439-3209551 | Rare:40 | ||||
| chr20:3407901-3408002 | Rare:29 | ||||
| chr20:3470933-3471091 | Common:1; Rare:76 | ||||
| chr20:3767720-3767991 | Common:3; Rare:85 | ||||
| chr20:3796101-3796311 | Rare:53 | ||||
| chr20:3889171-3889420 | Common:1; Rare:128; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:4148586-4148890 | Rare:85 |