| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45894864-45895136 | Common:1; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45899462-45899850 | Common:2; Rare:127 | ||||
| chr20:45902264-45902505 | Common:1; Rare:83 | ||||
| chr20:45971539-45971635 | Rare:27 | ||||
| chr20:46071915-46072221 | Rare:56 | ||||
| chr20:46100145-46100159 | Rare:1 | ||||
| chr20:47310523-47310784 | Common:1; Rare:57 | ||||
| chr20:47321740-47321850 | Rare:21 | ||||
| chr20:47334083-47334243 | Rare:38 | ||||
| chr20:47352548-47352665 | Rare:20 | ||||
| chr20:47358848-47358984 | Rare:32 | ||||
| chr20:47546552-47546852 | Rare:66 | ||||
| chr20:47639770-47640028 | Common:1; Rare:68 | ||||
| chr20:47717648-47717805 | Common:1; Rare:34 | ||||
| chr20:47791971-47792421 | Common:5; Rare:81 |