Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:380965-381079 | Common:2; Rare:32 | ||||
chr20:407913-408098 | Common:23; Rare:47 | ||||
chr20:543682-543915 | Rare:78 | ||||
chr20:1118448-1118677 | Common:3; Rare:72 | ||||
chr20:1393012-1393240 | Common:2; Rare:97 | ||||
chr20:2508894-2509222 | Rare:67 | ||||
chr20:2652434-2652661 | Common:8; Rare:80 | ||||
chr20:2664184-2664248 | Common:1; Rare:31 | ||||
chr20:3209447-3209534 | Rare:27 | ||||
chr20:3795706-3795804 | Common:2; Rare:29 | ||||
chr20:3846770-3846886 | Rare:36 | ||||
chr20:5119899-5120174 | Common:1; Rare:92 | ||||
chr20:5950408-5950702 | Common:8; Rare:92 | ||||
chr20:13784893-13785080 | Common:2; Rare:82; Clinvar (benign):3 | ||||
chr20:16573313-16573540 | Common:1; Rare:61 |