| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196503651-196504045 | Common:7; Rare:129 | ||||
| chr3:196568518-196568660 | Common:3; Rare:37 | ||||
| chr3:196639585-196639827 | Common:2; Rare:54 | ||||
| chr3:196712228-196712320 | Common:2; Rare:29 | ||||
| chr3:196867748-196867983 | Rare:85 | ||||
| chr3:196942375-196942686 | Common:1; Rare:131 | ||||
| chr3:197029779-197029938 | Common:1; Rare:51 | ||||
| chr3:197298571-197298687 | Rare:42 | ||||
| chr3:197299306-197299368 | Rare:8 | ||||
| chr3:197736784-197737140 | Common:3; Rare:108 | ||||
| chr3:197749748-197750018 | Common:1; Rare:95 | ||||
| chr3:197949893-197950251 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959979-197960272 | Common:1; Rare:107 | ||||
| chr4:337544-338012 | Common:7; Rare:141 | ||||
| chr4:499117-499333 | Common:3; Rare:88 |