| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084320-37084544 | Common:3; Rare:82 | ||||
| chr2:37231559-37231726 | Common:4; Rare:95; Clinvar (benign):4 | ||||
| chr2:37324731-37324943 | Common:1; Rare:89 | ||||
| chr2:38751340-38751491 | Rare:75 | ||||
| chr2:38875902-38876047 | Common:1; Rare:49 | ||||
| chr2:39437087-39437447 | Common:4; Rare:127 | ||||
| chr2:44361489-44361959 | Common:3; Rare:145 | ||||
| chr2:46617012-46617270 | Common:7; Rare:115 | ||||
| chr2:46915722-46915898 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916033-46916119 | Common:2; Rare:23 | ||||
| chr2:48314370-48314734 | Rare:134 | ||||
| chr2:53767740-53767866 | Common:1; Rare:45 | ||||
| chr2:53786862-53787184 | Common:1; Rare:120 | ||||
| chr2:53970788-53971113 | Common:9; Rare:106 | ||||
| chr2:55050302-55050397 | Rare:40 |