| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58389523-58389715 | Rare:65 | ||||
| chr20:58650987-58651345 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58652177-58652555 | Common:3; Rare:127 | ||||
| chr20:58692636-58692915 | Common:3; Rare:96 | ||||
| chr20:58888768-58889246 | Common:2; Rare:159 | ||||
| chr20:58890439-58890582 | Common:1; Rare:41 | ||||
| chr20:58890876-58891069 | Common:3; Rare:86 | ||||
| chr20:58891366-58891557 | Common:1; Rare:88; Clinvar:2 | ||||
| chr20:58892419-58892686 | Common:1; Rare:73 | ||||
| chr20:58981005-58981393 | Common:3; Rare:160 | ||||
| chr20:59006663-59006824 | Common:1; Rare:24 | ||||
| chr20:59006854-59007060 | Rare:52 | ||||
| chr20:59007062-59007127 | Rare:20 | ||||
| chr20:59032028-59032112 | Rare:26 | ||||
| chr20:59032269-59032677 | Common:6; Rare:170; Clinvar (benign):4 |