| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185282889-185283003 | Common:1; Rare:31 | ||||
| chr3:185586189-185586373 | Common:1; Rare:45 | ||||
| chr3:185824956-185825137 | Rare:58 | ||||
| chr3:185937938-185938220 | Common:2; Rare:125 | ||||
| chr3:186567281-186567485 | Common:3; Rare:57 | ||||
| chr3:186783287-186783617 | Common:1; Rare:142 | ||||
| chr3:186806402-186806541 | Rare:44 | ||||
| chr3:190513903-190514099 | Common:2; Rare:54 | ||||
| chr3:192917809-192918033 | Common:2; Rare:98 | ||||
| chr3:193240998-193241326 | Common:4; Rare:108 | ||||
| chr3:193593090-193593382 | Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194672153-194672482 | Common:2; Rare:99 | ||||
| chr3:196082075-196082228 | Common:1; Rare:64 | ||||
| chr3:196318184-196318340 | Common:1; Rare:65 | ||||
| chr3:196338397-196338711 | Rare:71 |