| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15099102-15099298 | Rare:50 | ||||
| chr3:15206152-15206588 | Common:1; Rare:177 | ||||
| chr3:15427401-15427629 | Common:1; Rare:71 | ||||
| chr3:15601382-15601806 | Common:4; Rare:172; Clinvar:1 | ||||
| chr3:15797764-15798047 | Common:1; Rare:49 | ||||
| chr3:15859720-15860121 | Common:4; Rare:129 | ||||
| chr3:16264787-16265268 | Common:4; Rare:167 | ||||
| chr3:17742485-17742946 | Common:4; Rare:158 | ||||
| chr3:19946887-19947436 | Common:10; Rare:199 | ||||
| chr3:20186088-20186341 | Common:3; Rare:73 | ||||
| chr3:23202926-23203226 | Common:1; Rare:106 | ||||
| chr3:23805715-23806063 | Common:3; Rare:71 | ||||
| chr3:23916853-23917224 | Rare:140 | ||||
| chr3:25428106-25428435 | Rare:76 | ||||
| chr3:25783377-25783640 | Common:2; Rare:85; Clinvar (benign):3 |