Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43530773-43530936 | Common:3; Rare:69 | ||||
chr1:43650000-43650185 | Rare:49 | ||||
chr1:43946585-43946983 | Rare:105 | ||||
chr1:43952951-43953238 | Rare:55 | ||||
chr1:43969794-43970018 | Rare:55 | ||||
chr1:43974808-43975130 | Common:4; Rare:83 | ||||
chr1:43979102-43979435 | Common:2; Rare:102 | ||||
chr1:44031133-44031397 | Common:3; Rare:56 | ||||
chr1:44213357-44213574 | Common:1; Rare:44 | ||||
chr1:44355267-44355470 | Common:1; Rare:46 | ||||
chr1:44631915-44632101 | Common:2; Rare:64 | ||||
chr1:44674381-44674765 | Common:3; Rare:110 | ||||
chr1:44775381-44775626 | Common:2; Rare:101 | ||||
chr1:44775811-44776140 | Common:2; Rare:118 | ||||
chr1:44986532-44986738 | Common:2; Rare:40; Clinvar (benign):1 |