Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42958823-42959042 | Common:3; Rare:60; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172053-43172344 | Common:3; Rare:113 | ||||
chr1:43307259-43307495 | Common:1; Rare:68 | ||||
chr1:43358662-43359128 | Common:7; Rare:140 | ||||
chr1:43367584-43367827 | Common:2; Rare:46 | ||||
chr1:43367915-43368208 | Rare:77 | ||||
chr1:43389757-43389950 | Common:3; Rare:86 | ||||
chr1:43649852-43650197 | Rare:86 | ||||
chr1:43946622-43946983 | Rare:98 | ||||
chr1:44213369-44213498 | Common:1; Rare:26 | ||||
chr1:44674424-44674717 | Common:3; Rare:77 | ||||
chr1:44775445-44775599 | Rare:59 | ||||
chr1:44808378-44808561 | Common:1; Rare:45 | ||||
chr1:45339937-45340243 | Common:1; Rare:114; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340408-45340451 | Common:1; Rare:8; Clinvar:1 |