| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48446612-48446743 | Rare:47 | ||||
| chr3:48504112-48504170 | Rare:22 | ||||
| chr3:48556712-48557192 | Common:1; Rare:116 | ||||
| chr3:48609378-48609736 | Common:1; Rare:121 | ||||
| chr3:48621740-48621808 | Rare:25 | ||||
| chr3:48635430-48635564 | Rare:43 | ||||
| chr3:48685820-48685953 | Common:1; Rare:54 | ||||
| chr3:48847663-48848005 | Common:1; Rare:94 | ||||
| chr3:48858606-48858753 | Rare:30; Clinvar (benign):1 | ||||
| chr3:48898820-48899009 | Rare:52; Clinvar:6 | ||||
| chr3:48918783-48918985 | Common:2; Rare:115 | ||||
| chr3:48973508-48973806 | Common:1; Rare:57 | ||||
| chr3:48982833-48982957 | Rare:22 | ||||
| chr3:48989728-48989901 | Rare:45 | ||||
| chr3:49006991-49007438 | Common:2; Rare:156 |