| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4979127-4979861 | Common:4; Rare:179 | ||||
| chr3:4979879-4979940 | Common:1; Rare:21 | ||||
| chr3:4980469-4980609 | Common:1; Rare:31 | ||||
| chr3:5122452-5122560 | Rare:22 | ||||
| chr3:5187302-5187735 | Common:5; Rare:172 | ||||
| chr3:8501532-8501955 | Common:3; Rare:156 | ||||
| chr3:9249626-9249747 | Common:1; Rare:34 | ||||
| chr3:9362948-9363145 | Common:2; Rare:67 | ||||
| chr3:9397431-9397933 | Common:1; Rare:156 | ||||
| chr3:9749797-9750076 | Common:1; Rare:88 | ||||
| chr3:9750169-9750369 | Common:1; Rare:79 | ||||
| chr3:9792301-9792596 | Rare:81 | ||||
| chr3:9792671-9793136 | Common:3; Rare:162 | ||||
| chr3:9839143-9839295 | Common:1; Rare:42; Clinvar (pathogenic):1 | ||||
| chr3:9890477-9890753 | Common:3; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 |