| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28394670-28394954 | Common:1; Rare:63 | ||||
| chr2:28471322-28471477 | Common:2; Rare:32 | ||||
| chr2:28600238-28600480 | Common:3; Rare:60 | ||||
| chr2:28625315-28625521 | Common:1; Rare:38 | ||||
| chr2:28793718-28793987 | Rare:45 | ||||
| chr2:28997355-28997532 | Common:1; Rare:35 | ||||
| chr2:32141778-32141941 | Rare:27; Clinvar (pathogenic):3 | ||||
| chr2:32358040-32358139 | Common:1; Rare:15 | ||||
| chr2:33555314-33555537 | Common:1; Rare:45 | ||||
| chr2:36509581-36509755 | Rare:23 | ||||
| chr2:36544142-36544495 | Common:3; Rare:101 | ||||
| chr2:36546978-36546988 | Rare:2 | ||||
| chr2:36548281-36548598 | Common:1; Rare:93 | ||||
| chr2:37216159-37216260 | Rare:30 | ||||
| chr2:37599769-37599964 | Common:5; Rare:45 |