| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196503688-196503945 | Common:5; Rare:88 | ||||
| chr3:196568527-196568673 | Common:3; Rare:37 | ||||
| chr3:196712188-196712578 | Common:5; Rare:128 | ||||
| chr3:196867749-196867938 | Rare:63 | ||||
| chr3:196942399-196942650 | Common:1; Rare:100 | ||||
| chr3:197736860-197737221 | Common:3; Rare:117 | ||||
| chr3:197791066-197791274 | Common:2; Rare:65 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197960083-197960244 | Common:1; Rare:65 | ||||
| chr4:53121-53348 | Rare:5 | ||||
| chr4:124289-124535 | Common:6; Rare:66 | ||||
| chr4:337528-337859 | Common:1; Rare:89 | ||||
| chr4:499141-499301 | Common:2; Rare:60 | ||||
| chr4:663588-663753 | Rare:56 | ||||
| chr4:674243-674566 | Common:2; Rare:152 |