| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45971846-45971891 | Rare:15 | ||||
| chr20:46118140-46118321 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46364386-46364709 | Common:2; Rare:108 | ||||
| chr20:47319040-47319135 | Common:1; Rare:32 | ||||
| chr20:47356682-47356873 | Rare:43 | ||||
| chr20:47501766-47502009 | Common:1; Rare:85 | ||||
| chr20:49278039-49278301 | Rare:73 | ||||
| chr20:50113112-50113244 | Common:5; Rare:65 | ||||
| chr20:50958487-50958830 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593787-53593914 | Common:1; Rare:49 | ||||
| chr20:54173977-54174124 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr20:56392187-56392385 | Rare:48 | ||||
| chr20:58651113-58651305 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:59042757-59043030 | Common:1; Rare:100 | ||||
| chr20:59940303-59940481 | Rare:73 |