Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44777611-44778116 | Common:2; Rare:126 | ||||
chr1:44808425-44808590 | Common:1; Rare:43 | ||||
chr1:45339996-45340048 | Rare:14 | ||||
chr1:45340103-45340193 | Rare:39 | ||||
chr1:45340388-45340488 | Common:1; Rare:26; Clinvar:1 | ||||
chr1:45499998-45500361 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521869-45522098 | Common:1; Rare:86 | ||||
chr1:45550719-45551110 | Common:3; Rare:96 | ||||
chr1:45583753-45584070 | Common:1; Rare:101 | ||||
chr1:45686466-45686651 | Rare:65 | ||||
chr1:45687057-45687357 | Common:1; Rare:78 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:46198389-46198506 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:46303138-46303769 | Common:3; Rare:188 | ||||
chr1:46340647-46340835 | Common:3; Rare:54 |