| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5126692-5127099 | Common:3; Rare:136 | ||||
| chr20:5610873-5611154 | Common:2; Rare:98 | ||||
| chr20:5750309-5750461 | Rare:37 | ||||
| chr20:5911306-5911628 | Common:3; Rare:88 | ||||
| chr20:5950391-5950720 | Common:8; Rare:101 | ||||
| chr20:6053976-6054182 | Common:1; Rare:37 | ||||
| chr20:9838829-9839184 | Common:3; Rare:98 | ||||
| chr20:10034854-10035155 | Common:6; Rare:113 | ||||
| chr20:10218727-10218939 | Rare:43 | ||||
| chr20:10219469-10219693 | Common:1; Rare:45 | ||||
| chr20:10434106-10434298 | Common:2; Rare:75; Clinvar (benign):1 | ||||
| chr20:10434448-10434688 | Common:1; Rare:73 | ||||
| chr20:10435073-10435369 | Rare:77 | ||||
| chr20:10673970-10674215 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:11890670-11890897 | Common:2; Rare:86 |