Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37808196-37808538 | Common:1; Rare:75 | ||||
chr1:38859712-38860043 | Rare:123 | ||||
chr1:38873312-38873551 | Common:3; Rare:83 | ||||
chr1:40257908-40258313 | Common:4; Rare:111; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40691504-40691731 | Common:1; Rare:113 | ||||
chr1:42456265-42456592 | Common:1; Rare:106 | ||||
chr1:42767016-42767301 | Common:4; Rare:88 | ||||
chr1:42816995-42817141 | Common:1; Rare:39 | ||||
chr1:42846420-42846638 | Common:1; Rare:57 | ||||
chr1:42958785-42959100 | Common:4; Rare:83; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172224-43172333 | Common:1; Rare:57 | ||||
chr1:43367961-43368212 | Rare:67 | ||||
chr1:43389736-43389909 | Common:3; Rare:73 | ||||
chr1:43707341-43707571 | Common:2; Rare:67 | ||||
chr1:43979880-43980020 | Common:2; Rare:34 |