| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100261166-100261730 | Common:8; Rare:390 | ||||
| chr3:100334483-100334883 | Common:8; Rare:417 | ||||
| chr3:100400810-100401277 | Common:2; Rare:470 | ||||
| chr3:100401274-100402021 | Common:9; Rare:457 | ||||
| chr3:100491957-100492357 | Common:2; Rare:113 | ||||
| chr3:100492370-100492672 | Common:10; Rare:478 | ||||
| chr3:100492697-100493097 | Common:9; Rare:71 | ||||
| chr3:100653912-100654318 | Common:6; Rare:245 | ||||
| chr3:100709052-100709672 | Common:54; Rare:1046; Clinvar (benign):6 | ||||
| chr3:100709683-100710083 | Common:3; Rare:82 | ||||
| chr3:100709989-100710218 | Common:3; Rare:75 | ||||
| chr3:101512261-101513452 | Common:68; Rare:780 | ||||
| chr3:101513534-101513934 | Common:1; Rare:71 | ||||
| chr3:101561630-101562110 | Common:15; Rare:555 | ||||
| chr3:101573501-101573860 | Common:1; Rare:143 |