| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28870267-28870429 | Rare:60 | ||||
| chr2:32039761-32039851 | Rare:27 | ||||
| chr2:32165690-32165893 | Common:1; Rare:76 | ||||
| chr2:37084340-37084544 | Common:3; Rare:74 | ||||
| chr2:37231551-37231702 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr2:37324738-37324915 | Common:1; Rare:71 | ||||
| chr2:38875902-38876043 | Common:1; Rare:46 | ||||
| chr2:46617012-46617257 | Common:6; Rare:105 | ||||
| chr2:46915738-46915885 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:48440619-48440815 | Common:6; Rare:81 | ||||
| chr2:53786862-53787080 | Rare:71 | ||||
| chr2:53970986-53971107 | Common:3; Rare:48 | ||||
| chr2:55519411-55519740 | Common:1; Rare:92 | ||||
| chr2:58046554-58046825 | Rare:77 | ||||
| chr2:58241344-58241396 | Rare:27; Clinvar:2; Clinvar (benign):1 |