Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43599333-43599530 | Common:2; Rare:38 | ||||
chr1:43605432-43605598 | Common:1; Rare:65 | ||||
chr1:43649871-43650204 | Rare:78 | ||||
chr1:43946548-43947022 | Rare:133 | ||||
chr1:43974587-43975042 | Common:3; Rare:107 | ||||
chr1:44031410-44031760 | Common:3; Rare:71 | ||||
chr1:44213348-44213549 | Common:1; Rare:40 | ||||
chr1:44218134-44218706 | Common:1; Rare:177 | ||||
chr1:44219828-44220134 | Common:3; Rare:77 | ||||
chr1:44631891-44632168 | Common:3; Rare:102 | ||||
chr1:44674413-44674744 | Common:3; Rare:88 | ||||
chr1:44739658-44739887 | Common:1; Rare:86 | ||||
chr1:44775438-44775615 | Common:2; Rare:70 | ||||
chr1:44775848-44776155 | Common:2; Rare:112 | ||||
chr1:44986532-44986825 | Common:2; Rare:58; Clinvar (benign):1 |