Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116373083-116373340 | Rare:86 | ||||
chr1:117929568-117929792 | Common:1; Rare:68 | ||||
chr1:119140640-119140764 | Rare:37 | ||||
chr1:120176377-120176596 | Rare:50 | ||||
chr1:145823937-145824249 | Rare:112 | ||||
chr1:145845553-145845636 | Common:2; Rare:22 | ||||
chr1:145918680-145919013 | Common:2; Rare:74 | ||||
chr1:145927430-145927644 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964755 | Rare:47 | ||||
chr1:145996567-145996850 | Common:1; Rare:107 | ||||
chr1:147172436-147172730 | Common:1; Rare:77 | ||||
chr1:147541258-147541569 | Common:1; Rare:48 | ||||
chr1:149812133-149812385 | Common:2; Rare:136 | ||||
chr1:149842746-149842954 | Rare:3 | ||||
chr1:149850848-149851062 | Rare:1 |