| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41947114-41947214 | Rare:31 | ||||
| chr22:42070761-42070961 | Common:2; Rare:44 | ||||
| chr22:42079505-42079771 | Common:2; Rare:72 | ||||
| chr22:42090643-42091049 | Common:2; Rare:168; Clinvar (pathogenic):1 | ||||
| chr22:42432345-42432477 | Rare:35 | ||||
| chr22:42614844-42615246 | Common:3; Rare:168 | ||||
| chr22:42646670-42646769 | Common:1; Rare:25 | ||||
| chr22:42649329-42649488 | Common:1; Rare:65 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 | ||||
| chr22:43812238-43812448 | Common:4; Rare:68 | ||||
| chr22:43955106-43955566 | Common:5; Rare:131 | ||||
| chr22:44181204-44181361 | Common:4; Rare:35 | ||||
| chr22:44312794-44313029 | Common:2; Rare:49 | ||||
| chr22:46053786-46053878 | Rare:33 | ||||
| chr22:46267878-46268037 | Common:1; Rare:50 |