| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52495282-52495416 | Common:1; Rare:40 | ||||
| chr3:52516577-52516730 | Rare:50 | ||||
| chr3:52535011-52535295 | Common:1; Rare:55 | ||||
| chr3:52685548-52685687 | Rare:42 | ||||
| chr3:52685792-52686202 | Common:3; Rare:149 | ||||
| chr3:52692998-52693542 | Common:5; Rare:178 | ||||
| chr3:52696033-52696083 | Common:1; Rare:15 | ||||
| chr3:52705554-52706282 | Common:4; Rare:238 | ||||
| chr3:52770889-52771007 | Common:3; Rare:35 | ||||
| chr3:53130405-53130523 | Common:1; Rare:39; Clinvar (benign):3 | ||||
| chr3:53347494-53347747 | Common:2; Rare:82 | ||||
| chr3:53846400-53846581 | Rare:59 | ||||
| chr3:53891779-53892045 | Common:2; Rare:84 | ||||
| chr3:56557081-56557245 | Common:2; Rare:64 | ||||
| chr3:56628490-56628698 | Common:1; Rare:45 |