| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126757-3127042 | Common:6; Rare:123; Clinvar (benign):4 | ||||
| chr3:3179663-3179890 | Common:2; Rare:81; Clinvar:3 | ||||
| chr3:3799196-3799476 | Common:2; Rare:110 | ||||
| chr3:4303253-4303425 | Common:1; Rare:66 | ||||
| chr3:4303607-4304041 | Common:5; Rare:272 | ||||
| chr3:4467206-4467315 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493101-4493520 | Common:2; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:5187326-5187712 | Common:5; Rare:156 | ||||
| chr3:5188392-5188836 | Common:4; Rare:195 | ||||
| chr3:8501520-8501980 | Common:3; Rare:161 | ||||
| chr3:8963419-8963614 | Common:1; Rare:57 | ||||
| chr3:9248372-9249188 | Common:3; Rare:269 | ||||
| chr3:9249446-9249762 | Common:2; Rare:69 | ||||
| chr3:9362917-9363241 | Common:5; Rare:88 | ||||
| chr3:9363343-9363459 | Rare:18 |