| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48847674-48847962 | Common:1; Rare:79 | ||||
| chr3:48918807-48918944 | Common:2; Rare:79 | ||||
| chr3:49007157-49007432 | Common:2; Rare:112 | ||||
| chr3:49021502-49021706 | Rare:52; Clinvar:1 | ||||
| chr3:49025128-49025540 | Common:1; Rare:93 | ||||
| chr3:49093990-49094071 | Rare:23 | ||||
| chr3:49104726-49104933 | Rare:84; Clinvar (benign):3 | ||||
| chr3:49166302-49166409 | Common:1; Rare:29 | ||||
| chr3:49340014-49340108 | Common:2; Rare:47 | ||||
| chr3:49411916-49412432 | Common:2; Rare:194 | ||||
| chr3:49689477-49689599 | Rare:37 | ||||
| chr3:49723942-49724285 | Common:9; Rare:120 | ||||
| chr3:49786504-49786799 | Common:2; Rare:94 | ||||
| chr3:49813845-49813991 | Common:1; Rare:22 | ||||
| chr3:50299240-50299692 | Common:2; Rare:107 |