| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21665948-21666070 | Rare:36 | ||||
| chr22:21867658-21867853 | Common:2; Rare:49 | ||||
| chr22:21982729-21982888 | Rare:46 | ||||
| chr22:22508704-22508913 | Rare:68 | ||||
| chr22:22520131-22520455 | Common:7; Rare:75 | ||||
| chr22:22558990-22559348 | Common:1; Rare:112 | ||||
| chr22:23767928-23768073 | Rare:38 | ||||
| chr22:23786874-23787121 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23856696-23856863 | Common:2; Rare:29 | ||||
| chr22:23857585-23857925 | Common:5; Rare:123 | ||||
| chr22:23894296-23894951 | Common:6; Rare:263; Clinvar:1 | ||||
| chr22:23974356-23974681 | Common:1; Rare:3 | ||||
| chr22:24011038-24011460 | Common:42; Rare:214 | ||||
| chr22:24270800-24271174 | Common:5; Rare:144 | ||||
| chr22:24555831-24556066 | Rare:71 |