| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:62060239-62060459 | Rare:38 | ||||
| chr3:62160889-62160910 | Rare:3 | ||||
| chr3:63863096-63863171 | Rare:16 | ||||
| chr3:64014333-64014492 | Rare:33 | ||||
| chr3:64016479-64016501 | Rare:5 | ||||
| chr3:64163432-64163549 | Common:3; Rare:24 | ||||
| chr3:64163878-64164029 | Common:5; Rare:32 | ||||
| chr3:64178538-64178842 | Common:1; Rare:51 | ||||
| chr3:65128408-65128685 | Common:3; Rare:53 | ||||
| chr3:65425025-65425101 | Rare:8 | ||||
| chr3:65580919-65580988 | Common:1; Rare:11 | ||||
| chr3:65583965-65584079 | Common:1; Rare:23 | ||||
| chr3:65866510-65866791 | Common:3; Rare:60 | ||||
| chr3:66394082-66394323 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr3:66798941-66799212 | Common:2; Rare:33 |