| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41170239-41170569 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41197421-41197594 | Common:1; Rare:41 | ||||
| chr22:41444411-41444551 | Common:1; Rare:34 | ||||
| chr22:41518261-41518570 | Common:3; Rare:62; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:41522684-41523240 | Rare:147; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr22:41524681-41524944 | Rare:76; Clinvar:1 | ||||
| chr22:41530687-41531045 | Common:2; Rare:124 | ||||
| chr22:41650476-41650883 | Rare:87 | ||||
| chr22:42060248-42060664 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:42083024-42083131 | Rare:16 | ||||
| chr22:42565141-42565171 | Rare:5 | ||||
| chr22:42587542-42587699 | Common:1; Rare:39 | ||||
| chr22:42587915-42588172 | Common:3; Rare:48 | ||||
| chr22:42601087-42601230 | Common:1; Rare:36 | ||||
| chr22:42613016-42613108 | Common:1; Rare:14 |