| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840631-2840788 | Common:1; Rare:64 | ||||
| chr20:2841136-2841257 | Common:2; Rare:22 | ||||
| chr20:2873357-2873481 | Common:2; Rare:38 | ||||
| chr20:3173526-3173699 | Common:1; Rare:62 | ||||
| chr20:3209464-3209542 | Rare:27 | ||||
| chr20:3407565-3407746 | Common:3; Rare:50 | ||||
| chr20:3407899-3407996 | Rare:29 | ||||
| chr20:3470872-3471040 | Common:2; Rare:78 | ||||
| chr20:3732550-3732768 | Rare:49 | ||||
| chr20:3795731-3795799 | Common:1; Rare:20 | ||||
| chr20:3796203-3796537 | Common:4; Rare:73 | ||||
| chr20:3820201-3820570 | Common:3; Rare:112 | ||||
| chr20:4686343-4686508 | Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:4823381-4823687 | Common:4; Rare:64 | ||||
| chr20:5112812-5113178 | Common:2; Rare:127 |