| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69541347-69541406 | Rare:8 | ||||
| chr3:69542477-69542811 | Common:3; Rare:92 | ||||
| chr3:71130527-71130685 | Rare:63; Clinvar:2 | ||||
| chr3:71581926-71582332 | Common:1; Rare:105 | ||||
| chr3:71725276-71725521 | Common:2; Rare:96 | ||||
| chr3:71754767-71754833 | Rare:11 | ||||
| chr3:71755018-71755303 | Rare:75 | ||||
| chr3:71784957-71785398 | Common:3; Rare:141; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:72848280-72848594 | Common:3; Rare:123 | ||||
| chr3:72996709-72997071 | Common:2; Rare:130 | ||||
| chr3:79018961-79019061 | Rare:31 | ||||
| chr3:81761515-81761873 | Common:8; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227255-87227404 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058180-88058742 | Common:2; Rare:156 | ||||
| chr3:88058914-88059321 | Common:3; Rare:157 |