| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651334-58651413 | Rare:16 | ||||
| chr20:58891151-58891433 | Common:4; Rare:116 | ||||
| chr20:58903526-58903778 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:58909130-58909423 | Common:3; Rare:76; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:58910334-58910729 | Common:2; Rare:86 | ||||
| chr20:58981098-58981364 | Common:2; Rare:118 | ||||
| chr20:59006987-59007077 | Rare:29 | ||||
| chr20:59032270-59032560 | Common:3; Rare:122; Clinvar (benign):4 | ||||
| chr20:59933612-59933792 | Common:4; Rare:71 | ||||
| chr20:59940291-59940494 | Rare:81 | ||||
| chr20:61252544-61252568 | Rare:4 | ||||
| chr20:62065823-62066056 | Common:2; Rare:101 | ||||
| chr20:62143283-62143809 | Common:7; Rare:223 | ||||
| chr20:62182945-62183052 | Rare:29 | ||||
| chr20:62301949-62302071 | Common:1; Rare:24 |