| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44885407-44885850 | Common:7; Rare:132 | ||||
| chr20:44960336-44960586 | Common:1; Rare:93 | ||||
| chr20:44966370-44966553 | Rare:74 | ||||
| chr20:45348332-45348597 | Common:2; Rare:83 | ||||
| chr20:45363109-45363221 | Rare:36 | ||||
| chr20:45363340-45363527 | Common:1; Rare:44 | ||||
| chr20:45791914-45791998 | Rare:34 | ||||
| chr20:45857299-45857633 | Common:4; Rare:94 | ||||
| chr20:45890998-45891400 | Common:4; Rare:123; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45912127-45912273 | Common:3; Rare:36 | ||||
| chr20:45934466-45934730 | Common:2; Rare:113 | ||||
| chr20:45971815-45972073 | Common:3; Rare:75 | ||||
| chr20:45972148-45972383 | Rare:93 | ||||
| chr20:46363940-46364064 | Common:1; Rare:21 | ||||
| chr20:46364330-46364544 | Common:1; Rare:79 |