Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43979947-43980006 | Common:2; Rare:12 | ||||
chr1:44674406-44674724 | Common:3; Rare:86 | ||||
chr1:44739674-44739889 | Common:1; Rare:82 | ||||
chr1:44775439-44775640 | Common:2; Rare:82 | ||||
chr1:44775838-44776140 | Common:2; Rare:109 | ||||
chr1:44800136-44800393 | Common:1; Rare:62 | ||||
chr1:44800531-44800676 | Rare:35 | ||||
chr1:44808403-44808561 | Common:1; Rare:39 | ||||
chr1:44986532-44986763 | Common:2; Rare:44; Clinvar (benign):1 | ||||
chr1:45011856-45012144 | Common:6; Rare:59; Clinvar (benign):1 | ||||
chr1:45340004-45340041 | Rare:6 | ||||
chr1:45340114-45340243 | Rare:56; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340579 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:45499960-45500350 | Common:2; Rare:91; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522093 | Common:1; Rare:101 |