| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38311317-38311461 | Rare:22 | ||||
| chr22:38327878-38328069 | Common:1; Rare:41 | ||||
| chr22:38336146-38336340 | Rare:53 | ||||
| chr22:38455819-38455956 | Common:1; Rare:20 | ||||
| chr22:38571001-38571115 | Rare:14 | ||||
| chr22:38696777-38697080 | Rare:56 | ||||
| chr22:38715475-38715661 | Rare:37 | ||||
| chr22:38768911-38769090 | Rare:45 | ||||
| chr22:38782544-38783118 | Common:3; Rare:117; Clinvar (benign):1 | ||||
| chr22:38788534-38788680 | Common:1; Rare:28 | ||||
| chr22:38796689-38796811 | Rare:22 | ||||
| chr22:38802741-38802920 | Common:2; Rare:37 | ||||
| chr22:38803016-38803067 | Common:1; Rare:9 | ||||
| chr22:38816795-38816982 | Rare:30 | ||||
| chr22:38873030-38873206 | Common:1; Rare:43 |