| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56801889-56802055 | Rare:60 | ||||
| chr3:57079257-57079388 | Common:2; Rare:42 | ||||
| chr3:57227604-57227899 | Common:3; Rare:101 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597326-57597661 | Common:4; Rare:106 | ||||
| chr3:57889885-57890100 | Rare:48; Clinvar (benign):2 | ||||
| chr3:58008344-58008433 | Common:1; Rare:32 | ||||
| chr3:58433805-58433935 | Rare:50; Clinvar (benign):2 | ||||
| chr3:58577360-58577655 | Common:2; Rare:50 | ||||
| chr3:62318925-62319079 | Rare:61 | ||||
| chr3:63443287-63443367 | Rare:16 | ||||
| chr3:63863747-63864104 | Common:7; Rare:117 | ||||
| chr3:63864446-63864546 | Common:2; Rare:38 | ||||
| chr3:64445413-64445598 | Common:1; Rare:48 | ||||
| chr3:66998010-66998351 | Common:2; Rare:84 |