| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9396638-9396689 | Rare:21 | ||||
| chr3:10925698-10926024 | Rare:80 | ||||
| chr3:12749758-12750074 | Common:2; Rare:89 | ||||
| chr3:14047128-14047244 | Rare:28 | ||||
| chr3:14125692-14125776 | Common:1; Rare:12 | ||||
| chr3:15738508-15738516 | Rare:1 | ||||
| chr3:30608371-30608482 | Common:1; Rare:19 | ||||
| chr3:30644545-30644820 | Rare:69; Clinvar:2; Clinvar (benign):5 | ||||
| chr3:37055085-37055331 | Rare:62 | ||||
| chr3:40453151-40453417 | Common:6; Rare:61 | ||||
| chr3:41225350-41225727 | Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:46692643-46692941 | Common:2; Rare:56 | ||||
| chr3:46986200-46986394 | Common:1; Rare:26 | ||||
| chr3:48433896-48434270 | Common:2; Rare:65 | ||||
| chr3:50157272-50157406 | Rare:28 |