| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38033415-38033807 | Common:2; Rare:116 | ||||
| chr20:38805596-38805754 | Common:2; Rare:35 | ||||
| chr20:38962168-38962382 | Common:1; Rare:92 | ||||
| chr20:40688840-40689140 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:41340549-41340874 | Common:1; Rare:79 | ||||
| chr20:43458264-43458418 | Common:2; Rare:59 | ||||
| chr20:43558920-43559099 | Rare:30 | ||||
| chr20:43590600-43590986 | Common:1; Rare:86 | ||||
| chr20:44210697-44211142 | Common:5; Rare:158 | ||||
| chr20:44311127-44311298 | Common:1; Rare:67 | ||||
| chr20:44475772-44475947 | Rare:76 | ||||
| chr20:44521929-44522243 | Common:2; Rare:97 | ||||
| chr20:44531821-44531978 | Common:1; Rare:50 | ||||
| chr20:44614415-44614670 | Rare:54 | ||||
| chr20:44651662-44651851 | Common:1; Rare:50; Clinvar (benign):1 |