| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25664308-25664433 | Rare:37 | ||||
| chr3:25664775-25665075 | Common:4; Rare:82 | ||||
| chr3:25783371-25783641 | Common:2; Rare:91; Clinvar (benign):3 | ||||
| chr3:25789957-25790130 | Common:5; Rare:70 | ||||
| chr3:28348607-28348747 | Rare:33 | ||||
| chr3:28348779-28349185 | Common:3; Rare:128 | ||||
| chr3:29280837-29281102 | Common:3; Rare:55 | ||||
| chr3:30606625-30606973 | Common:1; Rare:104; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:31532383-31532662 | Common:4; Rare:80 | ||||
| chr3:31981606-31981803 | Common:1; Rare:50 | ||||
| chr3:32106402-32106714 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238560-32238678 | Common:1; Rare:40 | ||||
| chr3:32487961-32488289 | Common:2; Rare:69 | ||||
| chr3:32570655-32570952 | Common:1; Rare:136 | ||||
| chr3:33097082-33097261 | Rare:58; Clinvar:2; Clinvar (benign):1 |