| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501738-47502004 | Common:1; Rare:96 | ||||
| chr20:48921604-48921808 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr20:49046173-49046402 | Common:3; Rare:73 | ||||
| chr20:49188119-49188395 | Common:2; Rare:101 | ||||
| chr20:49219200-49219512 | Common:1; Rare:134 | ||||
| chr20:49278026-49278239 | Rare:56 | ||||
| chr20:49278366-49278669 | Common:8; Rare:95 | ||||
| chr20:49713875-49714013 | Rare:49 | ||||
| chr20:49915429-49915545 | Rare:50 | ||||
| chr20:50113115-50113244 | Common:5; Rare:64 | ||||
| chr20:50958364-50958857 | Common:1; Rare:184; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:51562777-51563051 | Common:3; Rare:56 | ||||
| chr20:54173833-54174123 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:56358854-56359184 | Common:1; Rare:105 | ||||
| chr20:56392182-56392739 | Common:6; Rare:148 |