| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951056-40951419 | Common:2; Rare:124 | ||||
| chr22:40951600-40951738 | Common:1; Rare:39 | ||||
| chr22:41286175-41286428 | Common:2; Rare:75 | ||||
| chr22:41468945-41469149 | Rare:59 | ||||
| chr22:41621018-41621370 | Common:7; Rare:131 | ||||
| chr22:41947072-41947231 | Common:1; Rare:59 | ||||
| chr22:42079430-42079769 | Common:3; Rare:86 | ||||
| chr22:42614834-42615244 | Common:3; Rare:173 | ||||
| chr22:42649313-42649482 | Common:1; Rare:66 | ||||
| chr22:44024175-44024335 | Common:1; Rare:56 | ||||
| chr22:45163780-45163944 | Common:2; Rare:55 | ||||
| chr22:46250251-46250411 | Common:3; Rare:50 | ||||
| chr22:46296744-46296925 | Rare:59 | ||||
| chr22:49918387-49918726 | Common:1; Rare:132 | ||||
| chr22:50582784-50583124 | Common:7; Rare:106; Clinvar:2; Clinvar (benign):3 |