| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4303253-4303415 | Common:1; Rare:63 | ||||
| chr3:4467215-4467285 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493155-4493533 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4980280-4980517 | Rare:55 | ||||
| chr3:5187312-5187663 | Common:5; Rare:136 | ||||
| chr3:8501633-8501962 | Common:2; Rare:118 | ||||
| chr3:9249627-9249762 | Common:2; Rare:36 | ||||
| chr3:9362934-9363158 | Common:2; Rare:73 | ||||
| chr3:9397428-9397896 | Common:1; Rare:149 | ||||
| chr3:9749814-9750050 | Common:1; Rare:75 | ||||
| chr3:9769840-9770006 | Common:1; Rare:46 | ||||
| chr3:9792355-9792591 | Rare:67 | ||||
| chr3:9792705-9793123 | Common:3; Rare:148 | ||||
| chr3:9843957-9844136 | Common:2; Rare:74 |