Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44808403-44808561 | Common:1; Rare:39 | ||||
chr1:44986532-44986799 | Common:2; Rare:55; Clinvar (benign):1 | ||||
chr1:45340118-45340178 | Rare:22 | ||||
chr1:45500044-45500353 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522087 | Common:1; Rare:101 | ||||
chr1:45550720-45551082 | Common:3; Rare:89 | ||||
chr1:45583931-45584078 | Rare:57 | ||||
chr1:45687059-45687363 | Common:1; Rare:80 | ||||
chr1:45688055-45688216 | Common:1; Rare:41 | ||||
chr1:45750612-45750839 | Rare:82 | ||||
chr1:46198389-46198506 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:46203138-46203362 | Rare:37 | ||||
chr1:46303131-46303769 | Common:3; Rare:190 | ||||
chr1:46340664-46340821 | Common:3; Rare:41 | ||||
chr1:46604226-46604443 | Rare:54 |