| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5950414-5950696 | Common:8; Rare:86 | ||||
| chr20:10673964-10674127 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:13784854-13785080 | Common:3; Rare:98; Clinvar (benign):3 | ||||
| chr20:16573299-16573547 | Common:1; Rare:70 | ||||
| chr20:17226829-17227053 | Common:1; Rare:60 | ||||
| chr20:17558415-17558677 | Common:1; Rare:47 | ||||
| chr20:17558809-17558948 | Common:1; Rare:21 | ||||
| chr20:17569165-17569244 | Rare:19 | ||||
| chr20:17569838-17570219 | Common:5; Rare:143 | ||||
| chr20:17968406-17968599 | Common:4; Rare:77 | ||||
| chr20:17968784-17969129 | Common:3; Rare:122 | ||||
| chr20:18467023-18467109 | Rare:20 | ||||
| chr20:18467148-18467448 | Common:1; Rare:59 | ||||
| chr20:18507781-18507955 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:18567339-18567499 | Common:1; Rare:57 |