Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149850848-149851062 | Rare:1 | ||||
chr1:149886646-149887004 | Common:2; Rare:132 | ||||
chr1:149887894-149888305 | Rare:122 | ||||
chr1:149927754-149927900 | Common:1; Rare:60; Clinvar (benign):5 | ||||
chr1:150067671-150067866 | Rare:62 | ||||
chr1:150235928-150236356 | Common:1; Rare:95 | ||||
chr1:150257686-150257915 | Rare:52 | ||||
chr1:150258036-150258131 | Rare:20 | ||||
chr1:150272382-150272752 | Common:1; Rare:63 | ||||
chr1:150282285-150282602 | Common:3; Rare:67 | ||||
chr1:150293746-150293922 | Common:1; Rare:61 | ||||
chr1:150321421-150321592 | Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363928-150364201 | Common:4; Rare:96 | ||||
chr1:150364562-150364709 | Common:1; Rare:50 | ||||
chr1:150629087-150629398 | Common:1; Rare:99 |