| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:20186123-20186444 | Common:4; Rare:104 | ||||
| chr3:23202918-23203359 | Common:1; Rare:138 | ||||
| chr3:23805812-23806076 | Common:1; Rare:53 | ||||
| chr3:23810379-23810498 | Rare:33 | ||||
| chr3:23916848-23917359 | Rare:174 | ||||
| chr3:23917603-23917980 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr3:23944819-23944914 | Rare:25 | ||||
| chr3:24494795-24494959 | Rare:40 | ||||
| chr3:25664899-25665083 | Common:2; Rare:58 | ||||
| chr3:25783340-25783673 | Common:2; Rare:115; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:26694342-26694511 | Rare:32 | ||||
| chr3:27216437-27216616 | Common:1; Rare:28 | ||||
| chr3:27369170-27369579 | Common:1; Rare:96 | ||||
| chr3:27484077-27484302 | Common:2; Rare:73 |