Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19485451-19485762 | Rare:116 | ||||
chr1:19596854-19597068 | Common:2; Rare:97 | ||||
chr1:20486198-20486424 | Rare:52 | ||||
chr1:20508107-20508205 | Common:1; Rare:33 | ||||
chr1:20661346-20661702 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787259-20787490 | Rare:108 | ||||
chr1:21783103-21783272 | Common:2; Rare:62 | ||||
chr1:22451612-22451858 | Common:1; Rare:68 | ||||
chr1:23344233-23344521 | Common:2; Rare:93 | ||||
chr1:23368827-23368965 | Common:1; Rare:47 | ||||
chr1:23559444-23559628 | Common:1; Rare:81 | ||||
chr1:23691729-23691826 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23800745-23800948 | Common:1; Rare:67 | ||||
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:24642890-24643335 | Common:2; Rare:147 |