| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4467225-4467300 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493142-4493521 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979545-4979638 | Rare:18 | ||||
| chr3:5187299-5187663 | Common:5; Rare:139 | ||||
| chr3:8501627-8501937 | Common:2; Rare:115 | ||||
| chr3:9249627-9249753 | Common:1; Rare:35 | ||||
| chr3:9362930-9363144 | Common:2; Rare:70 | ||||
| chr3:9363287-9363406 | Rare:23 | ||||
| chr3:9397427-9397902 | Common:1; Rare:150 | ||||
| chr3:9649233-9649518 | Common:1; Rare:96 | ||||
| chr3:9731672-9731790 | Common:1; Rare:49 | ||||
| chr3:9749833-9750018 | Common:1; Rare:63 | ||||
| chr3:9750215-9750330 | Common:1; Rare:53 | ||||
| chr3:9792353-9792583 | Rare:66 | ||||
| chr3:9792692-9793124 | Common:3; Rare:152 |