| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840627-2840768 | Common:1; Rare:54 | ||||
| chr20:3173474-3173699 | Common:1; Rare:83 | ||||
| chr20:3204620-3204741 | Common:1; Rare:51 | ||||
| chr20:3209429-3209542 | Common:1; Rare:38 | ||||
| chr20:3407533-3407755 | Common:3; Rare:62 | ||||
| chr20:3470872-3471040 | Common:2; Rare:78 | ||||
| chr20:3767713-3767953 | Common:2; Rare:74 | ||||
| chr20:3795433-3795799 | Common:3; Rare:88 | ||||
| chr20:3846731-3846891 | Rare:48 | ||||
| chr20:4148712-4148891 | Rare:56 | ||||
| chr20:4686268-4686505 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:4823384-4823715 | Common:5; Rare:66 | ||||
| chr20:4823748-4823790 | Rare:11 | ||||
| chr20:5112883-5113144 | Common:1; Rare:101 | ||||
| chr20:5119903-5120155 | Common:1; Rare:87 |