| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25082067-25082467 | Common:7; Rare:196; Clinvar:8; Clinvar (benign):7 | ||||
| chr20:25195525-25195744 | Common:1; Rare:74 | ||||
| chr20:25247937-25248127 | Common:1; Rare:76 | ||||
| chr20:25390744-25391130 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):2 | ||||
| chr20:25407503-25407767 | Common:3; Rare:89 | ||||
| chr20:25585492-25585770 | Common:3; Rare:77 | ||||
| chr20:25623904-25624225 | Common:1; Rare:128 | ||||
| chr20:25696519-25696631 | Common:1; Rare:45 | ||||
| chr20:25696681-25697081 | Common:3; Rare:111 | ||||
| chr20:25861530-25861790 | Common:3; Rare:89 | ||||
| chr20:25863137-25863564 | Common:7; Rare:188 | ||||
| chr20:31514244-31514541 | Common:6; Rare:112 | ||||
| chr20:31547184-31547461 | Rare:69 | ||||
| chr20:31605103-31605311 | Common:7; Rare:87 | ||||
| chr20:31722546-31722679 | Rare:30 |