| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319601-39319776 | Common:3; Rare:78 | ||||
| chr22:40346454-40346556 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856752-40857154 | Common:2; Rare:149; Clinvar:3 | ||||
| chr22:41286164-41286428 | Common:2; Rare:80 | ||||
| chr22:41621012-41621375 | Common:7; Rare:134 | ||||
| chr22:42090668-42090945 | Common:2; Rare:126; Clinvar (pathogenic):1 | ||||
| chr22:42519790-42519920 | Common:1; Rare:49 | ||||
| chr22:42614853-42615246 | Common:3; Rare:162 | ||||
| chr22:42649322-42649660 | Common:8; Rare:110 | ||||
| chr22:42721165-42721370 | Common:1; Rare:50 | ||||
| chr22:43089401-43089496 | Common:1; Rare:21 | ||||
| chr22:43955304-43955560 | Common:3; Rare:76 | ||||
| chr22:44024189-44024335 | Common:1; Rare:54 | ||||
| chr22:45163844-45164003 | Common:2; Rare:57 | ||||
| chr22:46053794-46053885 | Rare:32 |