| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48635403-48635564 | Rare:53 | ||||
| chr3:48662905-48663017 | Rare:21 | ||||
| chr3:48847663-48847973 | Common:1; Rare:86 | ||||
| chr3:48918696-48918930 | Common:2; Rare:121 | ||||
| chr3:48989728-48989901 | Rare:45 | ||||
| chr3:49007155-49007426 | Common:2; Rare:111 | ||||
| chr3:49018491-49018625 | Rare:59 | ||||
| chr3:49021502-49021725 | Rare:55; Clinvar:1 | ||||
| chr3:49021992-49022174 | Rare:61; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49093466-49093643 | Rare:66 | ||||
| chr3:49093981-49094120 | Rare:35 | ||||
| chr3:49104417-49104568 | Rare:53; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:49104615-49104940 | Common:1; Rare:128; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120767-49121115 | Rare:97 | ||||
| chr3:49132824-49133161 | Rare:77; Clinvar:3 |