| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4303222-4303407 | Common:4; Rare:129 | ||||
| chr3:4303440-4303650 | Common:3; Rare:116 | ||||
| chr3:4467148-4467313 | Common:2; Rare:148; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:4493122-4493552 | Common:4; Rare:290; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:4978331-4978930 | Common:14; Rare:420 | ||||
| chr3:4979175-4979524 | Common:4; Rare:148 | ||||
| chr3:5187262-5187791 | Common:14; Rare:386 | ||||
| chr3:8501620-8501863 | Rare:164 | ||||
| chr3:8651987-8652190 | Common:2; Rare:87 | ||||
| chr3:8682035-8682167 | Common:3; Rare:35 | ||||
| chr3:8963298-8963901 | Common:11; Rare:314 | ||||
| chr3:9249616-9249742 | Common:1; Rare:56 | ||||
| chr3:9362936-9363242 | Common:8; Rare:165 | ||||
| chr3:9397431-9397953 | Common:2; Rare:311 | ||||
| chr3:9731060-9731540 | Common:8; Rare:212 |