| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319604-39319715 | Common:2; Rare:58 | ||||
| chr22:39532714-39533041 | Common:2; Rare:122 | ||||
| chr22:40346433-40346551 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41621018-41621339 | Common:6; Rare:120 | ||||
| chr22:42614885-42615256 | Common:3; Rare:152 | ||||
| chr22:42649333-42649479 | Common:1; Rare:56 | ||||
| chr22:43955303-43955562 | Common:3; Rare:79 | ||||
| chr22:45163684-45164003 | Common:4; Rare:116 | ||||
| chr22:46250270-46250404 | Common:1; Rare:43 | ||||
| chr22:46762517-46762628 | Common:3; Rare:40 | ||||
| chr22:50783628-50783843 | Common:1; Rare:64 | ||||
| chr3:3126773-3126985 | Common:4; Rare:91; Clinvar (benign):1 | ||||
| chr3:4979224-4979515 | Common:2; Rare:66 | ||||
| chr3:9362977-9363091 | Common:1; Rare:44 | ||||
| chr3:9397422-9397673 | Rare:85 |