| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193593106-193593360 | Rare:78; Clinvar:1 | ||||
| chr3:195543174-195543455 | Common:4; Rare:101 | ||||
| chr3:195892711-195892963 | Common:2; Rare:44 | ||||
| chr3:195895899-195896002 | Common:1; Rare:40 | ||||
| chr3:196082071-196082261 | Common:2; Rare:73 | ||||
| chr3:196287669-196287831 | Common:1; Rare:50 | ||||
| chr3:196318215-196318350 | Common:1; Rare:52 | ||||
| chr3:196432374-196432517 | Common:1; Rare:65 | ||||
| chr3:196867751-196867953 | Rare:71 | ||||
| chr3:196942382-196942686 | Common:1; Rare:126 | ||||
| chr3:197029780-197030056 | Common:2; Rare:79 | ||||
| chr3:197736833-197737128 | Common:3; Rare:92 | ||||
| chr3:197749769-197749962 | Common:1; Rare:73 | ||||
| chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959985-197960242 | Common:1; Rare:91 |