| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126775-3126990 | Common:4; Rare:94; Clinvar (benign):2 | ||||
| chr3:4303253-4303436 | Common:1; Rare:70 | ||||
| chr3:4493175-4493483 | Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4814440-4814875 | Common:7; Rare:109; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:4978637-4978932 | Common:3; Rare:89 | ||||
| chr3:4979419-4979726 | Common:2; Rare:77 | ||||
| chr3:4980283-4980605 | Common:1; Rare:77 | ||||
| chr3:5187374-5187663 | Common:5; Rare:117 | ||||
| chr3:8501666-8501937 | Common:2; Rare:99 | ||||
| chr3:9249617-9249816 | Common:2; Rare:46 | ||||
| chr3:9362993-9363098 | Rare:37 | ||||
| chr3:9397435-9397891 | Common:1; Rare:144 | ||||
| chr3:9749777-9749997 | Rare:75 | ||||
| chr3:9769881-9770037 | Common:1; Rare:42 | ||||
| chr3:9792369-9792570 | Rare:57 |