| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38201786-38202138 | Common:2; Rare:97 | ||||
| chr22:38398469-38398667 | Common:1; Rare:72 | ||||
| chr22:38505973-38506117 | Common:1; Rare:54 | ||||
| chr22:38506245-38506681 | Common:1; Rare:145 | ||||
| chr22:38570132-38570493 | Common:5; Rare:72 | ||||
| chr22:38656340-38656721 | Common:1; Rare:102 | ||||
| chr22:38681817-38682045 | Common:2; Rare:97 | ||||
| chr22:38738602-38738888 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:38755417-38755551 | Common:1; Rare:27 | ||||
| chr22:38872180-38872420 | Rare:64 | ||||
| chr22:38957409-38957612 | Rare:39 | ||||
| chr22:38982145-38982387 | Common:2; Rare:49 | ||||
| chr22:39014061-39014364 | Common:1; Rare:80 | ||||
| chr22:39020820-39020952 | Common:1; Rare:36 | ||||
| chr22:39244976-39245262 | Common:1; Rare:61 |