| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180989618-180989823 | Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793360-182793638 | Common:3; Rare:69 | ||||
| chr3:182980493-182980772 | Common:1; Rare:98 | ||||
| chr3:183099421-183099742 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253035-183253389 | Common:3; Rare:93 | ||||
| chr3:183555603-183555780 | Common:1; Rare:50 | ||||
| chr3:183635309-183635707 | Common:4; Rare:106 | ||||
| chr3:183884850-183884985 | Rare:50 | ||||
| chr3:184017856-184018059 | Rare:58 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184185856-184186210 | Common:5; Rare:133 | ||||
| chr3:184248875-184249032 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249504-184249777 | Common:1; Rare:86 | ||||
| chr3:184298944-184299330 | Common:5; Rare:120 | ||||
| chr3:184315003-184315324 | Common:1; Rare:91 |