| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916897-23917196 | Rare:116 | ||||
| chr3:25783391-25783750 | Common:2; Rare:100; Clinvar (benign):3 | ||||
| chr3:25789883-25790150 | Common:5; Rare:101 | ||||
| chr3:28348614-28348724 | Rare:27 | ||||
| chr3:28348793-28349116 | Common:2; Rare:104 | ||||
| chr3:31981603-31981815 | Common:1; Rare:55 | ||||
| chr3:32391413-32391720 | Common:1; Rare:54 | ||||
| chr3:32502795-32503114 | Rare:58 | ||||
| chr3:32570810-32570984 | Common:1; Rare:68 | ||||
| chr3:33096741-33096827 | Rare:26 | ||||
| chr3:33097113-33097260 | Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:33440854-33441046 | Common:2; Rare:37 | ||||
| chr3:33718174-33718329 | Rare:76 | ||||
| chr3:36908508-36908643 | Rare:27 | ||||
| chr3:36992713-36992799 | Rare:28 |