| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169773331-169773418 | Rare:25 | ||||
| chr3:170870175-170870274 | Rare:51 | ||||
| chr3:170908572-170908827 | Common:1; Rare:70 | ||||
| chr3:171460089-171460216 | Rare:31 | ||||
| chr3:171460229-171460512 | Common:1; Rare:62 | ||||
| chr3:171460756-171460959 | Rare:49 | ||||
| chr3:172711063-172711350 | Common:1; Rare:72 | ||||
| chr3:172750552-172750763 | Common:3; Rare:61 | ||||
| chr3:179071576-179071869 | Rare:82 | ||||
| chr3:179604620-179604904 | Common:2; Rare:117 | ||||
| chr3:180951230-180951388 | Rare:33 | ||||
| chr3:180989618-180989827 | Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183253823-183254117 | Common:1; Rare:87 | ||||
| chr3:183697670-183697921 | Common:2; Rare:109 | ||||
| chr3:183884837-183885039 | Common:1; Rare:70 |