| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5610856-5611163 | Common:2; Rare:149 | ||||
| chr20:5750291-5750453 | Rare:61 | ||||
| chr20:5950410-5950744 | Common:16; Rare:195 | ||||
| chr20:6005808-6006148 | Common:4; Rare:143 | ||||
| chr20:6122610-6122920 | Common:4; Rare:85; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:6122968-6123140 | Common:4; Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
| chr20:6123340-6123840 | Common:4; Rare:110; Clinvar:7; Clinvar (benign):3 | ||||
| chr20:6767419-6767713 | Common:2; Rare:216 | ||||
| chr20:8019739-8019930 | Rare:55 | ||||
| chr20:8131851-8132327 | Common:2; Rare:202 | ||||
| chr20:10034824-10035170 | Common:12; Rare:229 | ||||
| chr20:10218638-10218968 | Rare:121 | ||||
| chr20:10434109-10434276 | Common:4; Rare:123; Clinvar (benign):2 | ||||
| chr20:10434465-10434688 | Common:2; Rare:125 | ||||
| chr20:10435017-10435364 | Rare:123 |