| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73167921-73168150 | Rare:57 | ||||
| chr10:73210135-73210421 | Rare:62 | ||||
| chr10:73252594-73252791 | Rare:53; Clinvar:4 | ||||
| chr10:73495558-73495766 | Rare:42 | ||||
| chr10:73495803-73496145 | Common:2; Rare:95 | ||||
| chr10:73505307-73505581 | Common:2; Rare:60 | ||||
| chr10:73625850-73626118 | Rare:58 | ||||
| chr10:73641409-73641735 | Common:1; Rare:64 | ||||
| chr10:73655996-73656106 | Common:1; Rare:28 | ||||
| chr10:73743996-73744095 | Rare:30 | ||||
| chr10:73744246-73744430 | Common:1; Rare:49 | ||||
| chr10:73772182-73772326 | Common:3; Rare:57 | ||||
| chr10:73781966-73782110 | Common:1; Rare:49 | ||||
| chr10:73874492-73874743 | Rare:63 | ||||
| chr10:73997756-73998246 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):1 |