Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:94402694-94402986 | Common:2; Rare:112 | ||||
chr10:94545145-94545472 | Rare:59 | ||||
chr10:94545569-94545922 | Common:5; Rare:107 | ||||
chr10:95273699-95273874 | Rare:34 | ||||
chr10:95290510-95290604 | Rare:18 | ||||
chr10:95290608-95290817 | Common:2; Rare:51 | ||||
chr10:95290819-95291214 | Common:2; Rare:150 | ||||
chr10:95291242-95291322 | Common:1; Rare:20 | ||||
chr10:95561325-95561627 | Common:4; Rare:95 | ||||
chr10:95656310-95656556 | Common:3; Rare:61 | ||||
chr10:95656579-95657039 | Common:1; Rare:121; Clinvar:6; Clinvar (benign):4 | ||||
chr10:95693842-95694219 | Common:5; Rare:129; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907043-95907316 | Rare:61 | ||||
chr10:95907491-95907627 | Common:2; Rare:29 | ||||
chr10:95907832-95907961 | Common:2; Rare:41 |