| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23750900-23751451 | Common:27; Rare:788 | ||||
| chr22:23751383-23751894 | Common:7; Rare:158 | ||||
| chr22:23763498-23763898 | Common:4; Rare:139 | ||||
| chr22:23767630-23767830 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr22:23767850-23768280 | Rare:318 | ||||
| chr22:23768286-23768686 | Rare:118 | ||||
| chr22:23772605-23773005 | Common:1; Rare:170 | ||||
| chr22:23786688-23787145 | Common:14; Rare:376; Clinvar:13; Clinvar (benign):4 | ||||
| chr22:23787190-23787620 | Common:29; Rare:501; Clinvar:3; Clinvar (benign):16 | ||||
| chr22:23838986-23839453 | Common:3; Rare:405 | ||||
| chr22:23857627-23858047 | Common:13; Rare:458 | ||||
| chr22:23893587-23894015 | Common:1; Rare:71 | ||||
| chr22:23894014-23894890 | Common:34; Rare:1011; Clinvar:1 | ||||
| chr22:23894839-23895295 | Common:11; Rare:366 | ||||
| chr22:24010962-24011483 | Common:170; Rare:980 |