| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182793384-182793638 | Common:3; Rare:55 | ||||
| chr3:183099443-183099758 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183253039-183253310 | Common:3; Rare:78 | ||||
| chr3:183287423-183287806 | Common:1; Rare:67 | ||||
| chr3:183697680-183697909 | Common:2; Rare:104 | ||||
| chr3:183884727-183884969 | Rare:100 | ||||
| chr3:184017878-184018103 | Common:1; Rare:68 | ||||
| chr3:184135201-184135398 | Common:2; Rare:62; Clinvar:5 | ||||
| chr3:184176654-184176969 | Common:2; Rare:63 | ||||
| chr3:184185880-184186218 | Common:4; Rare:126 | ||||
| chr3:184248875-184249029 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249531-184249794 | Common:1; Rare:89 | ||||
| chr3:184298944-184299338 | Common:5; Rare:120 | ||||
| chr3:184314428-184314674 | Common:3; Rare:73 | ||||
| chr3:184325330-184325509 | Common:1; Rare:63 |