| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183099443-183099769 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183115994-183116260 | Common:3; Rare:66 | ||||
| chr3:183635507-183635707 | Common:2; Rare:63 | ||||
| chr3:183697671-183697949 | Common:2; Rare:115 | ||||
| chr3:183698044-183698171 | Rare:44 | ||||
| chr3:184017860-184018133 | Common:1; Rare:87 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184155208-184155604 | Common:1; Rare:116 | ||||
| chr3:184185849-184186210 | Common:5; Rare:135 | ||||
| chr3:184248875-184249021 | Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249489-184249797 | Common:1; Rare:97 | ||||
| chr3:184298944-184299279 | Common:3; Rare:103 | ||||
| chr3:184314412-184314663 | Common:3; Rare:74 | ||||
| chr3:184361590-184361822 | Rare:56 | ||||
| chr3:184711857-184712272 | Common:2; Rare:134 |