| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126813-3127017 | Common:4; Rare:94; Clinvar (benign):4 | ||||
| chr3:3799819-3799877 | Common:1; Rare:17 | ||||
| chr3:4303253-4303415 | Common:1; Rare:63 | ||||
| chr3:4493177-4493538 | Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979148-4979530 | Common:2; Rare:88 | ||||
| chr3:5187327-5187639 | Common:5; Rare:122 | ||||
| chr3:6862653-6862784 | Common:3; Rare:49 | ||||
| chr3:8501638-8501934 | Common:2; Rare:110 | ||||
| chr3:8963399-8963787 | Common:4; Rare:99 | ||||
| chr3:9249551-9249750 | Common:1; Rare:43 | ||||
| chr3:9362936-9363140 | Common:2; Rare:68 | ||||
| chr3:9397428-9397699 | Common:1; Rare:102 | ||||
| chr3:9749811-9750018 | Common:1; Rare:69 | ||||
| chr3:9792402-9792621 | Rare:57 | ||||
| chr3:9792732-9793123 | Common:3; Rare:135 |