| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942345-196942710 | Common:1; Rare:164 | ||||
| chr3:197029787-197029925 | Common:1; Rare:43 | ||||
| chr3:197736833-197737138 | Common:3; Rare:96 | ||||
| chr3:197749759-197750024 | Common:1; Rare:96 | ||||
| chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959969-197960259 | Common:1; Rare:100 | ||||
| chr4:337539-337837 | Common:1; Rare:70 | ||||
| chr4:499100-499284 | Common:3; Rare:71 | ||||
| chr4:663611-663723 | Rare:36 | ||||
| chr4:673362-673535 | Rare:68 | ||||
| chr4:674212-674588 | Common:4; Rare:173 | ||||
| chr4:730930-730975 | Rare:9 | ||||
| chr4:932239-932487 | Common:2; Rare:95 | ||||
| chr4:986930-987173 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113639 | Common:2; Rare:42 |