| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493165-4493538 | Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979201-4979501 | Common:2; Rare:63 | ||||
| chr3:4980284-4980517 | Rare:53 | ||||
| chr3:5187262-5187692 | Common:5; Rare:160 | ||||
| chr3:8501649-8501895 | Common:1; Rare:87 | ||||
| chr3:9249617-9249743 | Common:1; Rare:35 | ||||
| chr3:9362971-9363098 | Common:1; Rare:46 | ||||
| chr3:9397428-9397891 | Common:1; Rare:149 | ||||
| chr3:9749850-9750059 | Common:1; Rare:67 | ||||
| chr3:9769857-9769917 | Rare:13 | ||||
| chr3:9792382-9792610 | Rare:61 | ||||
| chr3:9792692-9793123 | Common:3; Rare:152 | ||||
| chr3:9890477-9890673 | Common:2; Rare:74 | ||||
| chr3:9902759-9902950 | Rare:56 | ||||
| chr3:9933503-9933863 | Common:2; Rare:145; Clinvar:3 |