| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:27090378-27090534 | Rare:33 | ||||
| chr3:27094875-27095086 | Rare:39 | ||||
| chr3:27590631-27591242 | Common:2; Rare:112 | ||||
| chr3:27632765-27632976 | Common:7; Rare:104 | ||||
| chr3:28349718-28349860 | Rare:38 | ||||
| chr3:29454405-29454656 | Common:3; Rare:35 | ||||
| chr3:30449407-30449666 | Rare:40 | ||||
| chr3:31423538-31423757 | Common:3; Rare:35 | ||||
| chr3:32146651-32146928 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:32420217-32420529 | Common:1; Rare:42 | ||||
| chr3:33612736-33612973 | Common:1; Rare:50 | ||||
| chr3:37017001-37017237 | Common:2; Rare:44 | ||||
| chr3:37163329-37163464 | Rare:22 | ||||
| chr3:37244171-37244295 | Common:2; Rare:33 | ||||
| chr3:37604395-37604680 | Common:1; Rare:46 |