| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45881063-45881241 | Common:2; Rare:39 | ||||
| chr20:45891192-45891387 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45896191-45896373 | Common:3; Rare:56 | ||||
| chr20:45910945-45911196 | Common:4; Rare:81 | ||||
| chr20:45911248-45911294 | Common:1; Rare:13 | ||||
| chr20:45911972-45912321 | Common:4; Rare:82 | ||||
| chr20:45934373-45934731 | Common:2; Rare:149 | ||||
| chr20:45935045-45935345 | Rare:118 | ||||
| chr20:45971734-45971946 | Common:3; Rare:70 | ||||
| chr20:46363926-46364081 | Common:1; Rare:30 | ||||
| chr20:46364362-46364528 | Rare:64 | ||||
| chr20:46406560-46406817 | Common:3; Rare:69 | ||||
| chr20:46513527-46513602 | Common:1; Rare:26 | ||||
| chr20:46689416-46689748 | Common:1; Rare:84 | ||||
| chr20:46709563-46709717 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 |