| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183555603-183555797 | Common:1; Rare:53 | ||||
| chr3:183635507-183635677 | Common:1; Rare:52 | ||||
| chr3:183697664-183697933 | Common:2; Rare:117 | ||||
| chr3:184017875-184018103 | Common:1; Rare:71 | ||||
| chr3:184135221-184135403 | Common:2; Rare:56; Clinvar:5 | ||||
| chr3:184185902-184186208 | Common:4; Rare:110 | ||||
| chr3:184248906-184249021 | Rare:54; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249527-184249707 | Rare:54 | ||||
| chr3:184298944-184299269 | Common:3; Rare:100 | ||||
| chr3:184314435-184314656 | Common:3; Rare:66 | ||||
| chr3:184361603-184361771 | Rare:45 | ||||
| chr3:184711953-184712074 | Rare:42 | ||||
| chr3:184812014-184812203 | Common:2; Rare:55 | ||||
| chr3:185282832-185283001 | Common:1; Rare:46 | ||||
| chr3:185586000-185586358 | Common:1; Rare:81 |