Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43389757-43389920 | Common:3; Rare:69 | ||||
chr1:43707348-43707608 | Common:2; Rare:77 | ||||
chr1:43946589-43946977 | Rare:103 | ||||
chr1:44739674-44739931 | Common:2; Rare:102 | ||||
chr1:44775499-44775599 | Rare:45 | ||||
chr1:44986532-44986730 | Common:2; Rare:38; Clinvar (benign):1 | ||||
chr1:45340004-45340182 | Rare:50 | ||||
chr1:45499993-45500351 | Common:2; Rare:84; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522093 | Common:1; Rare:101 | ||||
chr1:45583782-45584070 | Common:1; Rare:93 | ||||
chr1:45686515-45686651 | Rare:43 | ||||
chr1:45687041-45687380 | Common:1; Rare:91 | ||||
chr1:45688091-45688216 | Common:1; Rare:35 | ||||
chr1:46198389-46198518 | Common:1; Rare:51; Clinvar:1 | ||||
chr1:46303179-46303793 | Common:3; Rare:194 |