| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5112862-5113178 | Common:1; Rare:117 | ||||
| chr20:5119913-5120168 | Common:1; Rare:86 | ||||
| chr20:5126616-5126814 | Common:3; Rare:53 | ||||
| chr20:5911108-5911621 | Common:5; Rare:134 | ||||
| chr20:5950414-5950572 | Common:1; Rare:52 | ||||
| chr20:9514679-9514805 | Common:1; Rare:34 | ||||
| chr20:10218727-10218949 | Rare:45 | ||||
| chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr20:13995246-13995603 | Rare:102 | ||||
| chr20:16573308-16573547 | Common:1; Rare:67 | ||||
| chr20:17226770-17227058 | Common:1; Rare:81 | ||||
| chr20:17569949-17570210 | Common:3; Rare:115 | ||||
| chr20:17968788-17969119 | Common:3; Rare:118 | ||||
| chr20:18467010-18467110 | Rare:25 | ||||
| chr20:18467132-18467444 | Common:1; Rare:64 |