| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:32495240-32495678 | Common:2; Rare:119 | ||||
| chr7:33040899-33041150 | Common:1; Rare:43 | ||||
| chr7:33062681-33062916 | Common:3; Rare:96 | ||||
| chr7:33063116-33063215 | Common:1; Rare:34 | ||||
| chr7:33109249-33109532 | Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:33129217-33129592 | Common:5; Rare:108 | ||||
| chr7:33351790-33351862 | Rare:19 | ||||
| chr7:34939170-34939350 | Rare:43 | ||||
| chr7:35254077-35254224 | Common:1; Rare:45 | ||||
| chr7:35694449-35695271 | Common:5; Rare:207 | ||||
| chr7:35800543-35801513 | Common:4; Rare:329 | ||||
| chr7:35846673-35846881 | Rare:31 | ||||
| chr7:36153224-36153272 | Common:5; Rare:13 | ||||
| chr7:36366791-36366974 | Rare:56 | ||||
| chr7:36367158-36367427 | Rare:90 |