Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775833-44776140 | Common:2; Rare:112 | ||||
chr1:44777615-44778090 | Common:2; Rare:119 | ||||
chr1:44808425-44808561 | Rare:38 | ||||
chr1:44986525-44986744 | Common:2; Rare:42; Clinvar (benign):1 | ||||
chr1:45012145-45012262 | Rare:46; Clinvar:4 | ||||
chr1:45012612-45012786 | Common:1; Rare:33 | ||||
chr1:45339936-45340243 | Common:1; Rare:114; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340565 | Common:1; Rare:44; Clinvar:1 | ||||
chr1:45499960-45500359 | Common:2; Rare:92; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521800-45522089 | Common:1; Rare:108 | ||||
chr1:45550730-45551098 | Common:3; Rare:89 | ||||
chr1:45583879-45584198 | Common:2; Rare:119 | ||||
chr1:45686471-45686680 | Rare:79 | ||||
chr1:45687059-45687357 | Common:1; Rare:77 | ||||
chr1:45688097-45688259 | Common:1; Rare:50 |