| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840631-2840755 | Common:1; Rare:45 | ||||
| chr20:3045767-3046069 | Common:4; Rare:70 | ||||
| chr20:3209429-3209508 | Common:1; Rare:21 | ||||
| chr20:3767736-3768041 | Common:3; Rare:97 | ||||
| chr20:3846663-3846887 | Rare:64 | ||||
| chr20:3889161-3889362 | Rare:97; Clinvar:3 | ||||
| chr20:4823630-4823709 | Rare:11 | ||||
| chr20:5112994-5113177 | Rare:79 | ||||
| chr20:5119899-5120185 | Common:1; Rare:96 | ||||
| chr20:5610933-5611208 | Common:2; Rare:103 | ||||
| chr20:5950410-5950720 | Common:8; Rare:98 | ||||
| chr20:8600554-8600749 | Common:4; Rare:48 | ||||
| chr20:10673956-10674008 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr20:11890638-11890897 | Common:2; Rare:95 | ||||
| chr20:13638903-13639053 | Common:1; Rare:43 |