| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18970435-18970679 | Common:3; Rare:65 | ||||
| chr22:19171232-19171415 | Common:1; Rare:31 | ||||
| chr22:19171524-19171778 | Rare:96 | ||||
| chr22:19179473-19179657 | Common:1; Rare:41 | ||||
| chr22:19217988-19218213 | Common:2; Rare:48 | ||||
| chr22:19292342-19292393 | Rare:13 | ||||
| chr22:19663282-19663467 | Rare:23 | ||||
| chr22:19663990-19664260 | Rare:62 | ||||
| chr22:19681476-19681572 | Common:1; Rare:20 | ||||
| chr22:19766375-19766408 | Common:1; Rare:10; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:19855900-19855941 | Rare:6 | ||||
| chr22:19882096-19882171 | Rare:15 | ||||
| chr22:19886978-19887305 | Common:3; Rare:55 | ||||
| chr22:19891668-19891884 | Rare:44 | ||||
| chr22:19892079-19892281 | Common:1; Rare:52 |