| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437090-39437447 | Common:4; Rare:125 | ||||
| chr2:43595992-43596194 | Common:1; Rare:64 | ||||
| chr2:44361782-44362005 | Common:1; Rare:67 | ||||
| chr2:46617012-46617275 | Common:7; Rare:115 | ||||
| chr2:46915739-46916122 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176456-47176664 | Common:2; Rare:124; Clinvar (benign):4 | ||||
| chr2:47782956-47783210 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):10 | ||||
| chr2:53767559-53767881 | Common:5; Rare:114 | ||||
| chr2:53786922-53787079 | Rare:58 | ||||
| chr2:53970788-53971110 | Common:9; Rare:106 | ||||
| chr2:55050493-55050790 | Common:3; Rare:90 | ||||
| chr2:55232335-55232744 | Common:2; Rare:121 | ||||
| chr2:55269183-55269332 | Common:2; Rare:43 | ||||
| chr2:55519419-55519741 | Common:1; Rare:88 | ||||
| chr2:58046634-58046845 | Rare:64 |