Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859359-25859578 | Common:3; Rare:92 | ||||
chr1:26279952-26280192 | Rare:134 | ||||
chr1:26432119-26432415 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26900448-26900547 | Rare:32 | ||||
chr1:26921529-26921843 | Common:3; Rare:100 | ||||
chr1:26993530-26993693 | Common:4; Rare:44 | ||||
chr1:27322063-27322321 | Common:1; Rare:94 | ||||
chr1:28505795-28506050 | Common:2; Rare:95 | ||||
chr1:28643020-28643188 | Rare:65 | ||||
chr1:28736691-28737059 | Common:3; Rare:123 | ||||
chr1:31296743-31297139 | Common:5; Rare:120 | ||||
chr1:32200515-32200677 | Rare:37 | ||||
chr1:32222323-32222547 | Rare:91 | ||||
chr1:32291868-32292156 | Common:1; Rare:90 | ||||
chr1:32394418-32394643 | Common:1; Rare:60 |