| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18466689-18466853 | Rare:36 | ||||
| chr20:18466922-18467129 | Rare:50 | ||||
| chr20:18467136-18467507 | Common:3; Rare:91 | ||||
| chr20:18496606-18496884 | Common:1; Rare:49 | ||||
| chr20:18496967-18497044 | Common:1; Rare:15 | ||||
| chr20:18497120-18497380 | Common:2; Rare:90 | ||||
| chr20:18507311-18507989 | Common:4; Rare:185; Clinvar:6; Clinvar (benign):3 | ||||
| chr20:18567181-18567606 | Common:4; Rare:135 | ||||
| chr20:18567613-18567687 | Common:2; Rare:20 | ||||
| chr20:18587747-18588231 | Common:3; Rare:123 | ||||
| chr20:18588323-18588498 | Rare:40 | ||||
| chr20:20017067-20017391 | Rare:90 | ||||
| chr20:20052300-20052528 | Common:2; Rare:99 | ||||
| chr20:20052796-20052890 | Rare:26 | ||||
| chr20:20711870-20712090 | Common:1; Rare:36 |