| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23751323-23751463 | Rare:28 | ||||
| chr22:23754348-23754466 | Common:1; Rare:37 | ||||
| chr22:23763623-23763837 | Common:1; Rare:48 | ||||
| chr22:23767846-23768095 | Rare:69 | ||||
| chr22:23772681-23772900 | Rare:72 | ||||
| chr22:23786868-23787147 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23787186-23787586 | Common:7; Rare:142; Clinvar:1; Clinvar (benign):6 | ||||
| chr22:23838964-23839013 | Rare:20 | ||||
| chr22:23839098-23839485 | Common:2; Rare:111 | ||||
| chr22:23856802-23857119 | Common:9; Rare:93 | ||||
| chr22:23857123-23857245 | Common:1; Rare:30 | ||||
| chr22:23857381-23857504 | Rare:27 | ||||
| chr22:23857622-23857987 | Common:4; Rare:129 | ||||
| chr22:23894002-23894531 | Common:5; Rare:150 | ||||
| chr22:23894773-23895023 | Common:2; Rare:118; Clinvar:1 |