Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113904813-113905392 | Common:7; Rare:169; Clinvar (benign):1 | ||||
chr1:114716737-114716828 | Rare:44; Clinvar:3 | ||||
chr1:114757942-114758078 | Common:2; Rare:41 | ||||
chr1:114780628-114780841 | Common:1; Rare:71 | ||||
chr1:117929578-117929827 | Common:4; Rare:77 | ||||
chr1:119140634-119140743 | Rare:33 | ||||
chr1:145823937-145824260 | Rare:114 | ||||
chr1:145845542-145845636 | Common:3; Rare:24 | ||||
chr1:145918689-145919022 | Common:2; Rare:74 | ||||
chr1:145927422-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145957961-145958195 | Rare:57 | ||||
chr1:145964567-145964755 | Rare:47 | ||||
chr1:146938297-146938331 | Rare:15 | ||||
chr1:147172457-147172744 | Common:1; Rare:76 | ||||
chr1:149842746-149842954 | Rare:3 |