| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:18272284-18272569 | Common:1; Rare:56 | ||||
| chr12:18275865-18276040 | Common:1; Rare:35 | ||||
| chr12:18286689-18286930 | Common:1; Rare:49 | ||||
| chr12:18294166-18294236 | Rare:14 | ||||
| chr12:18313674-18314021 | Common:3; Rare:80; Clinvar:1 | ||||
| chr12:18349791-18349995 | Rare:41 | ||||
| chr12:18361249-18361535 | Common:2; Rare:43 | ||||
| chr12:18361794-18361961 | Rare:28 | ||||
| chr12:18394708-18394972 | Common:2; Rare:43 | ||||
| chr12:18399596-18399711 | Common:1; Rare:36 | ||||
| chr12:18411535-18411746 | Rare:29 | ||||
| chr12:18417171-18417342 | Rare:36 | ||||
| chr12:18429596-18429724 | Common:1; Rare:21 | ||||
| chr12:18444980-18444994 | Rare:2 | ||||
| chr12:18445585-18445727 | Rare:24 |