Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155173236-155173378 | Common:2; Rare:63 | ||||
chr1:155209123-155209245 | Rare:56 | ||||
chr1:155308649-155309006 | Rare:78 | ||||
chr1:155324208-155324568 | Common:2; Rare:134 | ||||
chr1:155859338-155859572 | Common:3; Rare:56 | ||||
chr1:156054611-156054871 | Common:3; Rare:72 | ||||
chr1:156134952-156135241 | Common:3; Rare:61; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:156136007-156136354 | Common:3; Rare:110; Clinvar:20; Clinvar (benign):14; Clinvar (pathogenic):8 | ||||
chr1:156282790-156282941 | Common:1; Rare:41 | ||||
chr1:156728394-156728488 | Common:1; Rare:20 | ||||
chr1:156728595-156728943 | Rare:99 | ||||
chr1:156767393-156767649 | Rare:75 | ||||
chr1:160343212-160343389 | Rare:68 | ||||
chr1:161045888-161046037 | Common:1; Rare:38 | ||||
chr1:161117954-161118141 | Rare:92 |