| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44319887-44320205 | Common:4; Rare:87 | ||||
| chr20:44407427-44407699 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr20:44692956-44693400 | Common:5; Rare:155 | ||||
| chr20:44696085-44696239 | Rare:43 | ||||
| chr20:44717751-44718340 | Common:7; Rare:173 | ||||
| chr20:44728694-44729134 | Common:9; Rare:174 | ||||
| chr20:45088292-45088719 | Common:4; Rare:100 | ||||
| chr20:47317320-47317566 | Common:2; Rare:95 | ||||
| chr20:47357534-47357916 | Common:2; Rare:120 | ||||
| chr20:47358820-47359040 | Rare:67 | ||||
| chr20:47359060-47359400 | Rare:123 | ||||
| chr20:47360797-47361032 | Common:4; Rare:87 | ||||
| chr20:47392010-47392400 | Common:5; Rare:103 | ||||
| chr20:47432440-47432940 | Common:7; Rare:159 | ||||
| chr20:50166051-50166340 | Common:2; Rare:143 |