| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50153651-50153939 | Common:2; Rare:119 | ||||
| chr20:50510071-50510427 | Common:3; Rare:138 | ||||
| chr20:50958488-50958896 | Common:1; Rare:153; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:51801468-51801581 | Common:2; Rare:29 | ||||
| chr20:51802278-51802781 | Common:2; Rare:133; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:53593561-53593926 | Common:3; Rare:145 | ||||
| chr20:54207814-54208120 | Rare:72 | ||||
| chr20:56392153-56392719 | Common:6; Rare:155 | ||||
| chr20:56468551-56468700 | Rare:69 | ||||
| chr20:57265756-57265914 | Common:1; Rare:58; Clinvar:1 | ||||
| chr20:57266004-57266306 | Common:1; Rare:80 | ||||
| chr20:57391934-57392084 | Common:5; Rare:28 | ||||
| chr20:58309431-58309715 | Common:2; Rare:111 | ||||
| chr20:58388987-58389325 | Common:4; Rare:171; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651144-58651305 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):1 |