Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43650325-43650472 | Rare:36 | ||||
chr1:43974788-43974976 | Common:3; Rare:53 | ||||
chr1:44674430-44674717 | Common:3; Rare:75 | ||||
chr1:44739674-44739878 | Common:1; Rare:77 | ||||
chr1:44775438-44775599 | Common:1; Rare:64 | ||||
chr1:44777624-44778116 | Common:2; Rare:124 | ||||
chr1:45340004-45340178 | Rare:48 | ||||
chr1:45500034-45500361 | Common:1; Rare:77; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521848-45522069 | Common:1; Rare:88 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688055-45688211 | Common:1; Rare:39 | ||||
chr1:45750622-45750816 | Rare:71 | ||||
chr1:46198415-46198522 | Common:1; Rare:42; Clinvar:1 | ||||
chr1:46303129-46303769 | Common:3; Rare:191 | ||||
chr1:46340678-46340814 | Common:3; Rare:35 |