Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43707337-43707571 | Common:2; Rare:69 | ||||
chr1:43946622-43946983 | Rare:98 | ||||
chr1:43974584-43975029 | Common:3; Rare:103 | ||||
chr1:44031405-44031668 | Common:2; Rare:53 | ||||
chr1:44213380-44213527 | Common:1; Rare:32 | ||||
chr1:44674401-44674824 | Common:3; Rare:112 | ||||
chr1:44723667-44723774 | Rare:22 | ||||
chr1:44739667-44739923 | Common:1; Rare:100 | ||||
chr1:44775445-44775615 | Common:1; Rare:65 | ||||
chr1:44775824-44776138 | Common:2; Rare:114 | ||||
chr1:44986512-44986784 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:45012554-45013018 | Common:1; Rare:127 | ||||
chr1:45014736-45015006 | Rare:84; Clinvar (pathogenic):4 | ||||
chr1:45326755-45326904 | Rare:35 | ||||
chr1:45339949-45340053 | Common:1; Rare:38; Clinvar (benign):1 |