Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160031828-160032071 | Common:2; Rare:63 | ||||
chr1:160098852-160099119 | Common:2; Rare:43 | ||||
chr1:160262439-160262604 | Rare:54 | ||||
chr1:160343181-160343399 | Rare:90 | ||||
chr1:160400393-160400615 | Common:1; Rare:54 | ||||
chr1:161038905-161039030 | Common:1; Rare:44 | ||||
chr1:161045888-161046066 | Common:1; Rare:47 | ||||
chr1:161117995-161118129 | Rare:65 | ||||
chr1:161132583-161132656 | Common:1; Rare:26 | ||||
chr1:161166268-161166511 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199053-161199304 | Rare:41 | ||||
chr1:161367866-161367913 | Rare:9 | ||||
chr1:161749592-161749829 | Rare:78 | ||||
chr1:161766164-161766365 | Common:3; Rare:60 | ||||
chr1:162497761-162497851 | Common:1; Rare:29 |