Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373276-234373780 | Common:1; Rare:218; Clinvar (benign):7 | ||||
chr1:234607904-234608337 | Common:4; Rare:144 | ||||
chr1:234608466-234608743 | Common:3; Rare:135; Clinvar (benign):2 | ||||
chr1:235128648-235129023 | Rare:150 | ||||
chr1:235327773-235327893 | Rare:37 | ||||
chr1:235328116-235328611 | Common:4; Rare:151 | ||||
chr1:235504420-235504727 | Common:4; Rare:90 | ||||
chr1:235866852-235867132 | Common:3; Rare:82 | ||||
chr1:236064897-236065367 | Common:4; Rare:162; Clinvar (pathogenic):1 | ||||
chr1:236281914-236282249 | Common:6; Rare:103 | ||||
chr1:236395236-236395521 | Rare:68 | ||||
chr1:236523886-236524041 | Common:2; Rare:40 | ||||
chr1:236540361-236540650 | Common:7; Rare:88 | ||||
chr1:236541385-236541702 | Common:13; Rare:77 | ||||
chr1:236604439-236604626 | Common:4; Rare:62 |