| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196639608-196639824 | Common:2; Rare:47 | ||||
| chr3:196712170-196712586 | Common:6; Rare:135 | ||||
| chr3:196867738-196867938 | Rare:65 | ||||
| chr3:196942322-196942904 | Common:1; Rare:257 | ||||
| chr3:197029767-197029987 | Common:1; Rare:64 | ||||
| chr3:197736870-197737239 | Common:3; Rare:117 | ||||
| chr3:197749795-197750041 | Common:1; Rare:90 | ||||
| chr3:197791102-197791290 | Common:2; Rare:68 | ||||
| chr3:197949880-197950533 | Common:7; Rare:183; Clinvar (benign):2 | ||||
| chr3:197950815-197950978 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959934-197960281 | Common:1; Rare:127 | ||||
| chr4:337431-337867 | Common:1; Rare:127 | ||||
| chr4:499124-499332 | Common:3; Rare:83 | ||||
| chr4:673862-673948 | Rare:43 | ||||
| chr4:674238-674566 | Common:2; Rare:154 |