Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45687016-45687372 | Common:2; Rare:98 | ||||
chr1:45688049-45688243 | Common:1; Rare:54 | ||||
chr1:45750599-45750823 | Rare:82 | ||||
chr1:45913561-45913642 | Rare:14 | ||||
chr1:46132614-46132777 | Rare:59 | ||||
chr1:46132874-46133244 | Common:3; Rare:103 | ||||
chr1:46175636-46175846 | Common:2; Rare:39 | ||||
chr1:46198331-46198534 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46203178-46203441 | Rare:63 | ||||
chr1:46303124-46303817 | Common:3; Rare:208 | ||||
chr1:46340562-46340827 | Common:5; Rare:68 | ||||
chr1:46604189-46604443 | Common:1; Rare:69 | ||||
chr1:46718493-46718575 | Common:2; Rare:16 | ||||
chr1:46810866-46811117 | Common:1; Rare:66 | ||||
chr1:47229328-47229641 | Rare:63 |