| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53347518-53347692 | Common:1; Rare:51 | ||||
| chr3:53846392-53846575 | Rare:61 | ||||
| chr3:53891794-53892040 | Common:2; Rare:76 | ||||
| chr3:56557076-56557228 | Common:2; Rare:57 | ||||
| chr3:56682995-56683359 | Common:4; Rare:124 | ||||
| chr3:57079247-57079347 | Rare:34 | ||||
| chr3:57227604-57227899 | Common:3; Rare:101 | ||||
| chr3:57555992-57556339 | Rare:89 | ||||
| chr3:57597288-57597762 | Common:4; Rare:136 | ||||
| chr3:58008524-58008691 | Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:58433769-58434018 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61251352-61251597 | Common:4; Rare:59 | ||||
| chr3:62318932-62319062 | Rare:50 | ||||
| chr3:63863747-63864134 | Common:7; Rare:127 | ||||
| chr3:63911996-63912112 | Rare:39 |