Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775783-44776140 | Common:2; Rare:131 | ||||
chr1:44800176-44800382 | Common:1; Rare:44 | ||||
chr1:44808405-44808573 | Common:1; Rare:39 | ||||
chr1:44986532-44986763 | Common:2; Rare:44; Clinvar (benign):1 | ||||
chr1:45012085-45012283 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339932-45340243 | Common:1; Rare:118; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340470 | Common:1; Rare:21; Clinvar:1 | ||||
chr1:45500056-45500359 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521800-45522089 | Common:1; Rare:108 | ||||
chr1:45550730-45551097 | Common:3; Rare:88 | ||||
chr1:45583931-45584155 | Rare:90 | ||||
chr1:45686479-45686649 | Rare:60 | ||||
chr1:45687016-45687353 | Common:2; Rare:90 | ||||
chr1:45688055-45688273 | Common:1; Rare:60 | ||||
chr1:45750621-45750817 | Rare:71 |