| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50732321-50732626 | Common:1; Rare:57 | ||||
| chr20:50902101-50902141 | Rare:9 | ||||
| chr20:58996638-58997014 | Common:4; Rare:99 | ||||
| chr20:59159419-59159656 | Rare:48 | ||||
| chr20:59163591-59163839 | Common:2; Rare:46 | ||||
| chr20:59831082-59831350 | Common:4; Rare:79 | ||||
| chr20:62123671-62123691 | Rare:1 | ||||
| chr20:62129489-62129834 | Common:2; Rare:66 | ||||
| chr20:62306371-62306733 | Common:3; Rare:132 | ||||
| chr20:62307134-62307449 | Common:1; Rare:100 | ||||
| chr20:62307459-62307564 | Common:1; Rare:37 | ||||
| chr20:62323778-62324101 | Common:2; Rare:98 | ||||
| chr20:62330842-62331171 | Common:3; Rare:122; Clinvar (pathogenic):1 | ||||
| chr20:62359186-62359327 | Rare:35 | ||||
| chr20:62362639-62362874 | Common:3; Rare:58 |