| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38033416-38033757 | Common:2; Rare:99 | ||||
| chr20:38926187-38926417 | Common:1; Rare:78 | ||||
| chr20:38962106-38962382 | Common:2; Rare:114 | ||||
| chr20:41028462-41028731 | Rare:75 | ||||
| chr20:43457805-43457907 | Rare:45 | ||||
| chr20:43590881-43590986 | Rare:28 | ||||
| chr20:43945573-43945926 | Common:3; Rare:86 | ||||
| chr20:44210745-44211121 | Common:5; Rare:130 | ||||
| chr20:44475791-44475896 | Rare:43 | ||||
| chr20:44909855-44910119 | Common:2; Rare:99 | ||||
| chr20:44966370-44966571 | Common:1; Rare:78 | ||||
| chr20:45416044-45416159 | Rare:31 | ||||
| chr20:45812306-45812698 | Common:4; Rare:112 | ||||
| chr20:45857337-45857616 | Common:3; Rare:73 | ||||
| chr20:45891247-45891379 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 |