| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158732153-158732383 | Common:8; Rare:71 | ||||
| chr3:158801976-158802153 | Common:2; Rare:81 | ||||
| chr3:159069256-159069395 | Rare:20 | ||||
| chr3:159763164-159763213 | Rare:11 | ||||
| chr3:159853020-159853295 | Rare:50 | ||||
| chr3:160399175-160399308 | Rare:35; Clinvar:2 | ||||
| chr3:160399494-160399676 | Rare:48; Clinvar:1 | ||||
| chr3:160565520-160565842 | Common:2; Rare:116 | ||||
| chr3:161104402-161104722 | Common:3; Rare:79 | ||||
| chr3:161105248-161105406 | Common:2; Rare:57 | ||||
| chr3:161221278-161221379 | Common:2; Rare:40 | ||||
| chr3:167734835-167735280 | Common:5; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735626-167735763 | Rare:37 | ||||
| chr3:169146327-169146405 | Rare:17 | ||||
| chr3:169146984-169147592 | Common:2; Rare:131 |