| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202238443-202238656 | Rare:75; Clinvar:1 | ||||
| chr2:202265655-202265808 | Rare:60 | ||||
| chr2:202377041-202377103 | Rare:17; Clinvar:1 | ||||
| chr2:202634872-202635012 | Common:4; Rare:45 | ||||
| chr2:202870772-202871008 | Common:2; Rare:61 | ||||
| chr2:202911892-202912571 | Common:4; Rare:187 | ||||
| chr2:203014672-203014931 | Common:1; Rare:78 | ||||
| chr2:203238779-203239058 | Common:3; Rare:104 | ||||
| chr2:203239285-203239320 | Rare:11 | ||||
| chr2:203328184-203328511 | Common:2; Rare:119 | ||||
| chr2:205682407-205682567 | Rare:30 | ||||
| chr2:206085771-206085960 | Common:1; Rare:54 | ||||
| chr2:206086141-206086294 | Rare:15 | ||||
| chr2:206159362-206160036 | Common:4; Rare:202; Clinvar (benign):1 | ||||
| chr2:206274504-206274788 | Common:1; Rare:87 |