| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264838-16265243 | Common:2; Rare:140 | ||||
| chr3:16512313-16512548 | Common:7; Rare:45 | ||||
| chr3:16512894-16513035 | Common:1; Rare:23 | ||||
| chr3:16513433-16513877 | Common:4; Rare:121 | ||||
| chr3:17742507-17742747 | Common:3; Rare:81 | ||||
| chr3:19946974-19947450 | Common:7; Rare:177 | ||||
| chr3:19975448-19975750 | Rare:77 | ||||
| chr3:21751082-21751417 | Common:4; Rare:107 | ||||
| chr3:23202925-23203207 | Common:1; Rare:100 | ||||
| chr3:23203259-23203426 | Rare:35 | ||||
| chr3:23916878-23917211 | Rare:129 | ||||
| chr3:23917648-23918029 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr3:24494722-24494889 | Rare:43 | ||||
| chr3:25428103-25428392 | Rare:65 | ||||
| chr3:25664886-25665068 | Common:1; Rare:59 |