| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41340549-41340883 | Common:1; Rare:80 | ||||
| chr20:43590650-43590986 | Rare:74 | ||||
| chr20:44187098-44187416 | Common:2; Rare:72 | ||||
| chr20:44187449-44187737 | Common:1; Rare:51 | ||||
| chr20:44210694-44211102 | Common:5; Rare:149 | ||||
| chr20:44475834-44475935 | Rare:42 | ||||
| chr20:44651687-44651839 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr20:44966391-44966539 | Rare:54 | ||||
| chr20:45406541-45406744 | Rare:52 | ||||
| chr20:45407065-45407335 | Common:1; Rare:43 | ||||
| chr20:45407860-45408221 | Common:2; Rare:72 | ||||
| chr20:45416026-45416170 | Rare:46 | ||||
| chr20:45791916-45792017 | Common:1; Rare:39 | ||||
| chr20:45834058-45834200 | Rare:49 | ||||
| chr20:45857334-45857614 | Common:3; Rare:75 |