| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184361524-184361937 | Rare:90 | ||||
| chr3:184711981-184712244 | Common:1; Rare:88 | ||||
| chr3:185282864-185283016 | Common:1; Rare:39 | ||||
| chr3:185498968-185499155 | Rare:66 | ||||
| chr3:185926303-185926738 | Common:2; Rare:97 | ||||
| chr3:185937878-185938283 | Common:2; Rare:162 | ||||
| chr3:186567294-186567434 | Common:3; Rare:36 | ||||
| chr3:186783260-186783646 | Common:1; Rare:170 | ||||
| chr3:186784349-186784520 | Rare:70 | ||||
| chr3:186806419-186806545 | Rare:40 | ||||
| chr3:186930411-186930617 | Common:1; Rare:55 | ||||
| chr3:187025211-187025489 | Common:1; Rare:40 | ||||
| chr3:188154082-188154215 | Rare:41 | ||||
| chr3:189631264-189631413 | Common:2; Rare:32 | ||||
| chr3:193593088-193593376 | Rare:95; Clinvar:2; Clinvar (benign):2 |