Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:20367513-20367594 | Common:1; Rare:29 | ||||
chr20:20369820-20370073 | Common:2; Rare:86 | ||||
chr20:20370287-20370439 | Rare:28 | ||||
chr20:20412870-20412985 | Common:1; Rare:17 | ||||
chr20:23025621-23025813 | Common:3; Rare:37 | ||||
chr20:25751081-25751215 | Rare:32 | ||||
chr20:25853988-25854116 | Common:3; Rare:48 | ||||
chr20:30580069-30580248 | Common:1; Rare:34 | ||||
chr20:33412046-33412311 | Rare:61; Clinvar (benign):1 | ||||
chr20:34709157-34709298 | Common:2; Rare:58 | ||||
chr20:36050087-36050164 | Common:1; Rare:22 | ||||
chr20:36050204-36050459 | Common:1; Rare:63 | ||||
chr20:36050498-36050737 | Common:1; Rare:93 | ||||
chr20:36050917-36051144 | Common:3; Rare:78 | ||||
chr20:37411588-37411821 | Common:17; Rare:81 |