| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197388-197628 | Common:3; Rare:61 | ||||
| chr3:3126784-3126990 | Common:4; Rare:87; Clinvar (benign):2 | ||||
| chr3:4303253-4303648 | Common:3; Rare:149 | ||||
| chr3:4493167-4493538 | Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979409-4979700 | Common:1; Rare:68 | ||||
| chr3:4980367-4980517 | Rare:39 | ||||
| chr3:5187287-5187718 | Common:5; Rare:164 | ||||
| chr3:8501620-8501937 | Common:2; Rare:120 | ||||
| chr3:9249605-9249757 | Common:1; Rare:37 | ||||
| chr3:9362934-9363132 | Common:2; Rare:67 | ||||
| chr3:9397430-9397896 | Common:1; Rare:148 | ||||
| chr3:9731442-9731814 | Common:3; Rare:121 | ||||
| chr3:9749789-9750088 | Common:1; Rare:93 | ||||
| chr3:9792375-9792596 | Rare:62 | ||||
| chr3:9792625-9793119 | Common:4; Rare:168 |