Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:50960203-50960361 | Rare:50 | ||||
chr1:50970070-50970309 | Common:1; Rare:44 | ||||
chr1:51236227-51236611 | Common:4; Rare:117 | ||||
chr1:51236832-51236898 | Rare:20 | ||||
chr1:51878621-51878949 | Common:1; Rare:93 | ||||
chr1:52055116-52055261 | Common:1; Rare:36 | ||||
chr1:52056078-52056379 | Common:2; Rare:79 | ||||
chr1:52141956-52142304 | Rare:81 | ||||
chr1:52404460-52404626 | Common:1; Rare:49 | ||||
chr1:52553444-52553692 | Common:3; Rare:70 | ||||
chr1:52698063-52698182 | Rare:29 | ||||
chr1:52698318-52698460 | Common:2; Rare:50 | ||||
chr1:52927237-52927365 | Common:2; Rare:43 | ||||
chr1:53196679-53196824 | Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
chr1:53220554-53220656 | Common:1; Rare:63 |