| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493165-4493532 | Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501638-8501926 | Common:2; Rare:107 | ||||
| chr3:9249610-9249757 | Common:1; Rare:36 | ||||
| chr3:9362942-9363127 | Common:2; Rare:67 | ||||
| chr3:9397437-9397873 | Common:1; Rare:140 | ||||
| chr3:9731438-9731814 | Common:3; Rare:122 | ||||
| chr3:9749811-9750007 | Rare:65 | ||||
| chr3:9792398-9792570 | Rare:47 | ||||
| chr3:9792705-9793124 | Common:3; Rare:148 | ||||
| chr3:9890503-9890673 | Common:2; Rare:62 | ||||
| chr3:9933517-9933870 | Common:2; Rare:145; Clinvar:3 | ||||
| chr3:10026329-10026480 | Rare:45 | ||||
| chr3:10115455-10115712 | Common:4; Rare:97 | ||||
| chr3:10321048-10321150 | Common:1; Rare:58 | ||||
| chr3:11719432-11719595 | Rare:51 |