Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:35049260-35049516 | Common:1; Rare:44 | ||||
chr21:36060508-36060613 | Common:3; Rare:35 | ||||
chr21:36134930-36135087 | Rare:41 | ||||
chr21:36320178-36320248 | Common:2; Rare:49 | ||||
chr21:36466461-36466524 | Rare:13 | ||||
chr21:36990212-36990237 | Common:2; Rare:13; Clinvar (benign):2 | ||||
chr21:37073015-37073348 | Common:5; Rare:132 | ||||
chr21:37267304-37267692 | Common:4; Rare:139 | ||||
chr21:38804943-38805179 | Common:2; Rare:63 | ||||
chr21:39380235-39380372 | Common:1; Rare:64 | ||||
chr21:41766973-41767242 | Common:6; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
chr21:42514418-42514498 | Rare:16 | ||||
chr21:42879041-42879167 | Rare:43 | ||||
chr21:42893064-42893336 | Common:4; Rare:88 | ||||
chr21:43659468-43659585 | Common:1; Rare:40 |