Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92029783-92030091 | Common:1; Rare:72 | ||||
chr1:92030381-92030417 | Rare:9 | ||||
chr1:92080186-92080356 | Rare:38 | ||||
chr1:92298908-92299137 | Common:1; Rare:109; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92792395-92792505 | Rare:22 | ||||
chr1:92831872-92832174 | Common:1; Rare:134; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92832238-92832528 | Rare:91 | ||||
chr1:92833237-92833484 | Rare:67; Clinvar (pathogenic):1 | ||||
chr1:92836290-92836583 | Rare:61 | ||||
chr1:93079089-93079979 | Common:4; Rare:236 | ||||
chr1:93117925-93117957 | Rare:5 | ||||
chr1:93120307-93120559 | Rare:50 | ||||
chr1:93120578-93120992 | Rare:69 | ||||
chr1:93179895-93180048 | Common:1; Rare:41 | ||||
chr1:93180053-93180255 | Rare:74 |