| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45890992-45891387 | Common:4; Rare:125; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45912140-45912310 | Common:3; Rare:38 | ||||
| chr20:46364386-46364527 | Rare:55 | ||||
| chr20:46689170-46689200 | Rare:6; Clinvar (pathogenic):1 | ||||
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:49219300-49219538 | Rare:111 | ||||
| chr20:49278029-49278241 | Rare:57 | ||||
| chr20:49568065-49568152 | Common:1; Rare:22 | ||||
| chr20:49915487-49915574 | Common:2; Rare:30 | ||||
| chr20:50113127-50113256 | Common:5; Rare:61 | ||||
| chr20:50131106-50131249 | Common:1; Rare:20 | ||||
| chr20:50958510-50958853 | Common:1; Rare:111; Clinvar (benign):2 | ||||
| chr20:53593802-53593894 | Common:1; Rare:34 | ||||
| chr20:56392182-56392697 | Common:6; Rare:136 | ||||
| chr20:57710553-57710740 | Common:1; Rare:53 |