| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24049592-24049754 | Rare:46 | ||||
| chr2:24076233-24076565 | Rare:93 | ||||
| chr2:24123255-24123478 | Common:1; Rare:55 | ||||
| chr2:26033785-26034159 | Common:3; Rare:133 | ||||
| chr2:26244597-26244984 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):7 | ||||
| chr2:26345791-26346160 | Common:1; Rare:111 | ||||
| chr2:26764230-26764305 | Rare:25 | ||||
| chr2:27032862-27033004 | Rare:55 | ||||
| chr2:27071604-27071872 | Common:1; Rare:83 | ||||
| chr2:27211910-27212023 | Common:3; Rare:43 | ||||
| chr2:27212252-27212371 | Common:1; Rare:59 | ||||
| chr2:27323031-27323129 | Rare:25; Clinvar (benign):1 | ||||
| chr2:27356750-27357080 | Rare:94 | ||||
| chr2:27370317-27370641 | Common:1; Rare:128 | ||||
| chr2:27628981-27629058 | Common:1; Rare:39 |