Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149850848-149851062 | Rare:1 | ||||
chr1:149886632-149887244 | Common:3; Rare:227 | ||||
chr1:149887933-149888233 | Rare:74 | ||||
chr1:149927756-149927901 | Common:1; Rare:60; Clinvar (benign):5 | ||||
chr1:150010507-150010837 | Common:4; Rare:74 | ||||
chr1:150067552-150067891 | Common:1; Rare:90 | ||||
chr1:150149381-150149666 | Rare:53 | ||||
chr1:150234642-150234742 | Rare:19 | ||||
chr1:150235906-150236366 | Common:1; Rare:103 | ||||
chr1:150257493-150257916 | Common:1; Rare:87 | ||||
chr1:150258036-150258121 | Rare:17 | ||||
chr1:150268362-150268463 | Rare:20 | ||||
chr1:150272368-150272747 | Common:1; Rare:65 | ||||
chr1:150282309-150282596 | Common:3; Rare:56 | ||||
chr1:150321359-150321608 | Rare:73; Clinvar:3; Clinvar (benign):1 |