Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19799864-19799978 | Common:2; Rare:43 | ||||
chr1:20652626-20652808 | Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
chr1:20661331-20661716 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786573-20786859 | Rare:106 | ||||
chr1:20787206-20787395 | Rare:94 | ||||
chr1:21290408-21290531 | Common:1; Rare:33 | ||||
chr1:21345463-21345674 | Common:2; Rare:80 | ||||
chr1:21440036-21440189 | Common:1; Rare:34 | ||||
chr1:21783086-21783277 | Common:2; Rare:69 | ||||
chr1:21847750-21848006 | Common:2; Rare:93; Clinvar:3 | ||||
chr1:21854711-21854872 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
chr1:22451752-22451883 | Rare:49 | ||||
chr1:23019345-23019537 | Rare:70 | ||||
chr1:23368207-23368503 | Common:1; Rare:87 | ||||
chr1:23369367-23369554 | Rare:82 |