| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23805451-23806148 | Common:4; Rare:182 | ||||
| chr3:23916841-23917218 | Rare:267 | ||||
| chr3:23917480-23917880 | Common:5; Rare:167 | ||||
| chr3:23945142-23945403 | Common:12; Rare:169 | ||||
| chr3:24494682-24494945 | Rare:108 | ||||
| chr3:24495160-24495560 | Common:10; Rare:171 | ||||
| chr3:25664015-25664206 | Common:2; Rare:49 | ||||
| chr3:25664875-25665063 | Common:1; Rare:60 | ||||
| chr3:25782943-25783128 | Rare:40 | ||||
| chr3:25783375-25783656 | Common:4; Rare:167; Clinvar (benign):6 | ||||
| chr3:25789900-25790132 | Common:9; Rare:149 | ||||
| chr3:27484277-27484736 | Common:4; Rare:148 | ||||
| chr3:28241433-28241791 | Common:4; Rare:242 | ||||
| chr3:28348300-28348580 | Common:4; Rare:105 | ||||
| chr3:28348580-28348770 | Rare:82 |