| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38962131-38962382 | Common:1; Rare:104 | ||||
| chr20:43457816-43457907 | Rare:42 | ||||
| chr20:43590650-43590996 | Rare:78 | ||||
| chr20:44210708-44211009 | Common:4; Rare:109 | ||||
| chr20:44475777-44475910 | Rare:55 | ||||
| chr20:44885415-44885780 | Common:7; Rare:113 | ||||
| chr20:44960350-44960542 | Common:1; Rare:72 | ||||
| chr20:45416018-45416153 | Rare:36 | ||||
| chr20:45812330-45812709 | Common:4; Rare:108 | ||||
| chr20:45857343-45857614 | Common:3; Rare:70 | ||||
| chr20:45891174-45891387 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934618-45934707 | Rare:46 | ||||
| chr20:46406571-46406814 | Common:2; Rare:63 | ||||
| chr20:47356666-47356887 | Rare:51 | ||||
| chr20:47501764-47501929 | Common:1; Rare:59 |