| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3045868-3046098 | Common:2; Rare:62 | ||||
| chr20:3209433-3209542 | Common:1; Rare:37 | ||||
| chr20:3767730-3768051 | Common:4; Rare:102 | ||||
| chr20:3820468-3820572 | Rare:43 | ||||
| chr20:4686209-4686496 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:4823593-4823709 | Rare:18 | ||||
| chr20:5112972-5113168 | Rare:84 | ||||
| chr20:5119874-5120174 | Common:1; Rare:101 | ||||
| chr20:5610938-5611208 | Common:2; Rare:100 | ||||
| chr20:5950410-5950691 | Common:8; Rare:87 | ||||
| chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr20:16573321-16573540 | Common:1; Rare:59 | ||||
| chr20:16729849-16730064 | Rare:64 | ||||
| chr20:17968453-17968594 | Common:4; Rare:59 | ||||
| chr20:17968770-17969119 | Common:4; Rare:125 |