| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35875553-35875851 | Common:4; Rare:46 | ||||
| chr20:36050290-36050459 | Common:1; Rare:46 | ||||
| chr20:36050498-36050732 | Common:1; Rare:90 | ||||
| chr20:36050880-36051098 | Common:2; Rare:80 | ||||
| chr20:36606920-36607017 | Rare:19 | ||||
| chr20:37379287-37379440 | Common:1; Rare:27 | ||||
| chr20:38446536-38446736 | Common:1; Rare:67 | ||||
| chr20:41005428-41005690 | Rare:41 | ||||
| chr20:41643696-41643829 | Common:2; Rare:32 | ||||
| chr20:41693281-41693615 | Common:2; Rare:64 | ||||
| chr20:44911569-44911653 | Rare:17 | ||||
| chr20:45894708-45895009 | Common:3; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:47357794-47357892 | Rare:15 | ||||
| chr20:47358848-47358977 | Rare:28 | ||||
| chr20:47360838-47361008 | Common:2; Rare:42 |