Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147541401-147541518 | Rare:15 | ||||
chr1:148458684-148459006 | Common:2; Rare:90 | ||||
chr1:148952279-148952603 | Common:5; Rare:97 | ||||
chr1:149812349-149812591 | Rare:71 | ||||
chr1:149842746-149842908 | Rare:3 | ||||
chr1:149850848-149851062 | Rare:1 | ||||
chr1:149886612-149887004 | Common:2; Rare:150 | ||||
chr1:149887873-149888061 | Rare:78 | ||||
chr1:150067600-150067886 | Common:1; Rare:79 | ||||
chr1:150321413-150321590 | Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150579595-150579785 | Common:4; Rare:51 | ||||
chr1:150629466-150629825 | Rare:77 | ||||
chr1:150926289-150926455 | Rare:48 | ||||
chr1:151070517-151070793 | Common:2; Rare:79 | ||||
chr1:151165840-151166162 | Common:3; Rare:87 |