Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145957992-145958212 | Rare:50 | ||||
chr1:145964495-145964742 | Rare:60 | ||||
chr1:147172457-147172779 | Common:1; Rare:82 | ||||
chr1:147242409-147242706 | Common:4; Rare:91 | ||||
chr1:149812217-149812527 | Common:2; Rare:143 | ||||
chr1:149850848-149851068 | Rare:1 | ||||
chr1:149886515-149887147 | Common:3; Rare:247 | ||||
chr1:149887904-149888217 | Rare:96 | ||||
chr1:149927775-149927918 | Common:1; Rare:48; Clinvar (benign):4 | ||||
chr1:150067610-150067844 | Common:1; Rare:64 | ||||
chr1:150282296-150282597 | Common:3; Rare:60 | ||||
chr1:150293810-150293914 | Rare:36 | ||||
chr1:150364572-150364717 | Common:1; Rare:51 | ||||
chr1:150579596-150579846 | Common:9; Rare:77 |