Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19485460-19485765 | Rare:116 | ||||
chr1:19596891-19597094 | Common:2; Rare:100 | ||||
chr1:20508079-20508236 | Common:2; Rare:56 | ||||
chr1:20661349-20661750 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786647-20786861 | Rare:87 | ||||
chr1:20787196-20787533 | Rare:158 | ||||
chr1:21176852-21177173 | Common:1; Rare:95 | ||||
chr1:21345463-21345704 | Common:3; Rare:90 | ||||
chr1:21783082-21783293 | Common:2; Rare:77 | ||||
chr1:22052544-22052742 | Common:2; Rare:66 | ||||
chr1:22451749-22451868 | Rare:48 | ||||
chr1:23344214-23344544 | Common:2; Rare:114 | ||||
chr1:23368207-23368243 | Rare:9 | ||||
chr1:23368843-23369130 | Common:1; Rare:77 | ||||
chr1:23424648-23424863 | Rare:63 |