Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39632942-39633216 | Common:1; Rare:68 | ||||
chr1:40388575-40388738 | Rare:38 | ||||
chr1:40394955-40395031 | Common:1; Rare:12 | ||||
chr1:43348871-43349118 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
chr1:44644732-44645073 | Common:2; Rare:72 | ||||
chr1:44778669-44778875 | Common:1; Rare:55 | ||||
chr1:44780743-44780753 | Rare:2 | ||||
chr1:45205844-45205950 | Common:1; Rare:33 | ||||
chr1:46032360-46032623 | Rare:76 | ||||
chr1:46718315-46718518 | Common:1; Rare:43 | ||||
chr1:58782971-58783012 | Rare:19 | ||||
chr1:58783073-58783360 | Common:3; Rare:75 | ||||
chr1:58783547-58783681 | Rare:28 | ||||
chr1:58903728-58903809 | Rare:24 | ||||
chr1:59056474-59056644 | Common:2; Rare:40 |