| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45174676-45174905 | Rare:53 | ||||
| chr20:45363364-45363512 | Common:1; Rare:34 | ||||
| chr20:45406537-45406726 | Rare:50 | ||||
| chr20:45416042-45416335 | Rare:113; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45791913-45792007 | Common:1; Rare:38 | ||||
| chr20:45848692-45848806 | Common:1; Rare:26 | ||||
| chr20:45857315-45857633 | Common:3; Rare:90 | ||||
| chr20:45890345-45890637 | Common:1; Rare:100 | ||||
| chr20:45891165-45891432 | Common:1; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45897563-45897755 | Rare:38 | ||||
| chr20:45934466-45934734 | Common:2; Rare:115 | ||||
| chr20:45935053-45935351 | Rare:115 | ||||
| chr20:45971733-45971983 | Common:3; Rare:77 | ||||
| chr20:46364368-46364544 | Rare:66 | ||||
| chr20:46406565-46406779 | Common:2; Rare:54 |