| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:2098649-2098962 | Common:4; Rare:125 | ||||
| chr3:3126784-3126990 | Common:4; Rare:87; Clinvar (benign):2 | ||||
| chr3:4303253-4303424 | Common:1; Rare:66 | ||||
| chr3:4303443-4303651 | Common:2; Rare:75 | ||||
| chr3:4493167-4493538 | Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979154-4979641 | Common:3; Rare:110 | ||||
| chr3:8501613-8501941 | Common:2; Rare:125 | ||||
| chr3:9249633-9249743 | Common:1; Rare:34 | ||||
| chr3:9362978-9363117 | Common:1; Rare:53 | ||||
| chr3:9397427-9397723 | Common:1; Rare:107 | ||||
| chr3:9749726-9750041 | Common:1; Rare:101 | ||||
| chr3:9769853-9770057 | Common:1; Rare:51 | ||||
| chr3:9792381-9792611 | Rare:62 | ||||
| chr3:9792685-9793123 | Common:3; Rare:155 | ||||
| chr3:9843968-9844132 | Common:2; Rare:65 |