| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:62506131-62506340 | Common:1; Rare:81 | ||||
| chr2:63588226-63589149 | Common:2; Rare:291; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:63840824-63841154 | Common:2; Rare:91 | ||||
| chr2:63841678-63842103 | Common:1; Rare:121 | ||||
| chr2:64018977-64019268 | Common:1; Rare:78 | ||||
| chr2:64019414-64019530 | Rare:43 | ||||
| chr2:64524098-64524436 | Common:3; Rare:109 | ||||
| chr2:64653730-64654071 | Common:1; Rare:114 | ||||
| chr2:64750307-64750626 | Rare:65 | ||||
| chr2:64988353-64988498 | Rare:27 | ||||
| chr2:64989091-64989430 | Common:7; Rare:86 | ||||
| chr2:64989511-64989790 | Common:5; Rare:84; Clinvar:2 | ||||
| chr2:65056154-65056462 | Common:2; Rare:106 | ||||
| chr2:65227579-65227955 | Rare:101 | ||||
| chr2:66434795-66435610 | Common:3; Rare:175 |