| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41919305-41919413 | Common:2; Rare:15 | ||||
| chr22:41919844-41920214 | Common:2; Rare:90 | ||||
| chr22:41920363-41920521 | Common:1; Rare:26 | ||||
| chr22:41920592-41920651 | Rare:11 | ||||
| chr22:41920662-41920885 | Rare:38 | ||||
| chr22:41924364-41924609 | Common:5; Rare:44 | ||||
| chr22:41924893-41925137 | Rare:40 | ||||
| chr22:41925523-41925893 | Common:4; Rare:92 | ||||
| chr22:41926162-41926243 | Common:1; Rare:27; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:41929647-41929738 | Rare:24 | ||||
| chr22:41931753-41931811 | Rare:5 | ||||
| chr22:41936189-41936581 | Common:1; Rare:78 | ||||
| chr22:41941338-41941648 | Common:1; Rare:57 | ||||
| chr22:41945793-41945877 | Rare:12 | ||||
| chr22:41947899-41948036 | Rare:26 |