Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36450412-36450601 | Common:1; Rare:55 | ||||
chr1:36463929-36464126 | Common:5; Rare:45 | ||||
chr1:36464144-36464503 | Common:3; Rare:118 | ||||
chr1:36472354-36472673 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:36473568-36473870 | Common:2; Rare:83; Clinvar (benign):1 | ||||
chr1:36482819-36483039 | Common:1; Rare:47 | ||||
chr1:37474348-37474595 | Common:1; Rare:97 | ||||
chr1:37514718-37514844 | Common:1; Rare:78 | ||||
chr1:37556809-37557036 | Common:2; Rare:91 | ||||
chr1:37595785-37596070 | Common:2; Rare:99 | ||||
chr1:37634567-37634743 | Common:1; Rare:55 | ||||
chr1:37690433-37690757 | Common:7; Rare:94 | ||||
chr1:37692229-37692489 | Common:3; Rare:54 | ||||
chr1:37808284-37808633 | Common:1; Rare:82 | ||||
chr1:37859541-37859842 | Common:4; Rare:108 |