Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91021454-91021687 | Common:4; Rare:101 | ||||
chr1:91021932-91022348 | Rare:199 | ||||
chr1:91404788-91404993 | Common:2; Rare:65 | ||||
chr1:91885928-91886385 | Rare:299 | ||||
chr1:91906271-91906405 | Rare:36 | ||||
chr1:92029744-92030670 | Common:11; Rare:360 | ||||
chr1:92298927-92299074 | Common:2; Rare:139; Clinvar:4; Clinvar (benign):2 | ||||
chr1:92485874-92486390 | Common:2; Rare:142 | ||||
chr1:92486838-92487062 | Common:2; Rare:106 | ||||
chr1:92784993-92785291 | Common:7; Rare:212 | ||||
chr1:92831872-92832142 | Common:2; Rare:234; Clinvar:14; Clinvar (benign):14 | ||||
chr1:92961407-92961633 | Rare:160 | ||||
chr1:93079071-93079354 | Common:5; Rare:215 | ||||
chr1:93179790-93180020 | Common:2; Rare:87 | ||||
chr1:93180228-93180762 | Common:4; Rare:400 |