| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58111859-58112168 | Common:1; Rare:65; Clinvar:2 | ||||
| chr3:58112182-58112473 | Rare:84; Clinvar:2 | ||||
| chr3:58117342-58117945 | Common:4; Rare:98 | ||||
| chr3:58124327-58124770 | Common:6; Rare:122; Clinvar:3; Clinvar (benign):4 | ||||
| chr3:58131092-58131547 | Common:3; Rare:86 | ||||
| chr3:58133143-58133427 | Common:3; Rare:42 | ||||
| chr3:58140913-58141076 | Rare:20 | ||||
| chr3:58141760-58142272 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:58144481-58144736 | Common:2; Rare:50 | ||||
| chr3:58159536-58159889 | Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:58160767-58161070 | Common:1; Rare:55 | ||||
| chr3:58162023-58162095 | Rare:10 | ||||
| chr3:58166647-58166736 | Rare:19 | ||||
| chr3:58170161-58170710 | Common:4; Rare:143; Clinvar:2 | ||||
| chr3:58182089-58182221 | Common:2; Rare:31 |