| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:53786856-53787191 | Common:1; Rare:128 | ||||
| chr2:53859948-53860216 | Common:1; Rare:69 | ||||
| chr2:53970725-53971168 | Common:12; Rare:170 | ||||
| chr2:54115435-54115678 | Rare:78 | ||||
| chr2:54456073-54456427 | Common:2; Rare:137 | ||||
| chr2:55050199-55050763 | Common:5; Rare:181 | ||||
| chr2:55232249-55232726 | Common:3; Rare:134 | ||||
| chr2:55519452-55519870 | Common:2; Rare:137 | ||||
| chr2:55544047-55544267 | Rare:69 | ||||
| chr2:58046403-58046721 | Rare:91 | ||||
| chr2:58046746-58046875 | Common:2; Rare:45 | ||||
| chr2:58047224-58047407 | Rare:55 | ||||
| chr2:60756150-60756303 | Rare:54 | ||||
| chr2:60881315-60881687 | Common:2; Rare:135 | ||||
| chr2:61017420-61017762 | Common:1; Rare:105; Clinvar:2; Clinvar (benign):2 |