Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:41035390-41035524 | Common:2; Rare:29 | ||||
chr1:41039761-41039899 | Rare:19 | ||||
chr1:41118064-41118127 | Rare:4 | ||||
chr1:41164562-41164748 | Rare:30 | ||||
chr1:42940346-42940583 | Common:2; Rare:50 | ||||
chr1:43232072-43232390 | Common:3; Rare:41 | ||||
chr1:43435303-43435395 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr1:43619074-43619456 | Rare:134 | ||||
chr1:44216427-44216592 | Common:1; Rare:33 | ||||
chr1:44217069-44217195 | Common:1; Rare:22 | ||||
chr1:44649683-44649910 | Rare:70 | ||||
chr1:44780743-44780750 | Rare:2 | ||||
chr1:44844466-44844566 | Common:1; Rare:17 | ||||
chr1:45205844-45205962 | Common:1; Rare:38 | ||||
chr1:45303559-45303914 | Common:1; Rare:99 |