| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23767920-23768019 | Rare:27 | ||||
| chr22:23857830-23857964 | Common:4; Rare:47 | ||||
| chr22:23894292-23894847 | Common:6; Rare:214; Clinvar:1 | ||||
| chr22:24270580-24270999 | Common:4; Rare:135 | ||||
| chr22:24554957-24555498 | Common:4; Rare:202 | ||||
| chr22:24555731-24556067 | Rare:103 | ||||
| chr22:26483768-26483917 | Common:4; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512413-26512576 | Common:2; Rare:67 | ||||
| chr22:26590063-26590220 | Common:3; Rare:68 | ||||
| chr22:27919155-27919565 | Common:5; Rare:171 | ||||
| chr22:28741776-28742090 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):7 | ||||
| chr22:28742436-28742722 | Common:1; Rare:66 | ||||
| chr22:28800274-28800714 | Common:6; Rare:153 | ||||
| chr22:29267852-29268348 | Common:2; Rare:145 | ||||
| chr22:29553551-29553820 | Rare:86 |