| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26034339-26034588 | Common:2; Rare:65 | ||||
| chr2:26244592-26244973 | Common:2; Rare:139; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345798-26346156 | Common:1; Rare:107 | ||||
| chr2:26764210-26764369 | Common:1; Rare:58 | ||||
| chr2:27032862-27033009 | Rare:57 | ||||
| chr2:27211920-27212106 | Common:3; Rare:71 | ||||
| chr2:27212225-27212370 | Common:1; Rare:77 | ||||
| chr2:27263028-27263181 | Rare:38 | ||||
| chr2:27323043-27323129 | Rare:19; Clinvar (benign):1 | ||||
| chr2:27356738-27356863 | Rare:33 | ||||
| chr2:27356961-27357199 | Common:2; Rare:87 | ||||
| chr2:27370275-27370681 | Common:2; Rare:167 | ||||
| chr2:27582969-27583101 | Rare:50 | ||||
| chr2:27628981-27629098 | Common:1; Rare:64 | ||||
| chr2:27663369-27663469 | Rare:28 |