| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26034526-26034639 | Rare:42 | ||||
| chr2:26244581-26244984 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345802-26346160 | Common:1; Rare:108 | ||||
| chr2:26764193-26764347 | Common:2; Rare:61 | ||||
| chr2:27032841-27033004 | Rare:66 | ||||
| chr2:27051542-27051706 | Rare:49 | ||||
| chr2:27071545-27071898 | Common:1; Rare:106 | ||||
| chr2:27086557-27086790 | Rare:66 | ||||
| chr2:27211737-27212088 | Common:3; Rare:119 | ||||
| chr2:27212225-27212370 | Common:1; Rare:77 | ||||
| chr2:27217215-27217485 | Rare:105 | ||||
| chr2:27323063-27323143 | Rare:20 | ||||
| chr2:27356743-27357150 | Common:1; Rare:118 | ||||
| chr2:27370275-27370641 | Common:1; Rare:151 | ||||
| chr2:27489643-27489958 | Rare:84; Clinvar (benign):1 |