| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421511-74421797 | Rare:90 | ||||
| chr2:74439950-74440063 | Rare:21 | ||||
| chr2:74440543-74440694 | Rare:37 | ||||
| chr2:74440750-74441060 | Rare:43 | ||||
| chr2:74454831-74455120 | Rare:79 | ||||
| chr2:74458092-74458458 | Common:1; Rare:108 | ||||
| chr2:74465315-74465541 | Common:2; Rare:62; Clinvar:1 | ||||
| chr2:74472391-74472769 | Common:4; Rare:176 | ||||
| chr2:74482088-74482224 | Rare:56 | ||||
| chr2:74482903-74483122 | Common:1; Rare:80 | ||||
| chr2:74483240-74483540 | Common:2; Rare:102 | ||||
| chr2:74502922-74503322 | Common:3; Rare:130 | ||||
| chr2:74507280-74507540 | Rare:75 | ||||
| chr2:74507640-74507829 | Rare:46 | ||||
| chr2:74529048-74529448 | Common:3; Rare:211; Clinvar (benign):1 |