| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651131-58651305 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651614-58651933 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:58688959-58689125 | Common:2; Rare:28 | ||||
| chr20:58840342-58840588 | Common:1; Rare:94; Clinvar:2 | ||||
| chr20:58840616-58840742 | Rare:46 | ||||
| chr20:58852520-58852732 | Rare:55 | ||||
| chr20:58852948-58852991 | Rare:13 | ||||
| chr20:58888788-58888999 | Common:1; Rare:63 | ||||
| chr20:58981163-58981318 | Common:2; Rare:80 | ||||
| chr20:59042726-59043041 | Common:1; Rare:116 | ||||
| chr20:59933632-59933792 | Common:4; Rare:64 | ||||
| chr20:59940224-59940481 | Rare:103 | ||||
| chr20:62143256-62143829 | Common:7; Rare:240 | ||||
| chr20:62182942-62183049 | Rare:29 | ||||
| chr20:62386953-62387136 | Common:3; Rare:80 |