| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49046176-49046387 | Common:3; Rare:68 | ||||
| chr20:49278031-49278248 | Rare:57 | ||||
| chr20:50190530-50190846 | Rare:91 | ||||
| chr20:50958468-50958834 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:56392187-56392545 | Common:3; Rare:97 | ||||
| chr20:56468423-56468762 | Rare:112 | ||||
| chr20:58309418-58309731 | Common:2; Rare:119 | ||||
| chr20:58651043-58651298 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr20:58909163-58909422 | Common:3; Rare:58; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr20:58909950-58910371 | Rare:98 | ||||
| chr20:59940314-59940489 | Rare:71 | ||||
| chr20:62065878-62066054 | Common:2; Rare:72 | ||||
| chr20:62143301-62143775 | Common:6; Rare:200 | ||||
| chr20:62238233-62238584 | Common:1; Rare:96 | ||||
| chr20:62386924-62387133 | Common:3; Rare:94 |