| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804401-42804763 | Common:4; Rare:112 | ||||
| chr3:43621919-43622316 | Common:2; Rare:117; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690792-43691004 | Common:3; Rare:114; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338019-44338192 | Common:2; Rare:53 | ||||
| chr3:44338384-44338458 | Rare:26 | ||||
| chr3:44338675-44338800 | Common:3; Rare:47 | ||||
| chr3:44477609-44477752 | Common:1; Rare:36 | ||||
| chr3:44510611-44510923 | Common:5; Rare:71 | ||||
| chr3:44555125-44555232 | Rare:24 | ||||
| chr3:44584703-44584986 | Rare:52 | ||||
| chr3:44624913-44625118 | Common:3; Rare:56 | ||||
| chr3:44712578-44712704 | Common:1; Rare:49 | ||||
| chr3:44729521-44729676 | Common:1; Rare:59 | ||||
| chr3:44761552-44761817 | Common:3; Rare:108 | ||||
| chr3:44861757-44861925 | Common:2; Rare:76 |