Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92848360-92848536 | Rare:65 | ||||
chr10:93702356-93702755 | Common:5; Rare:123 | ||||
chr10:93757677-93758028 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr10:93893872-93894031 | Common:1; Rare:65 | ||||
chr10:94362897-94363041 | Common:3; Rare:60 | ||||
chr10:94402276-94402441 | Rare:39 | ||||
chr10:94545668-94545888 | Common:4; Rare:74 | ||||
chr10:95561338-95561761 | Common:4; Rare:118 | ||||
chr10:95693891-95694217 | Common:5; Rare:102; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:95907733-95907964 | Common:3; Rare:67 | ||||
chr10:96043428-96043583 | Common:1; Rare:59 | ||||
chr10:96129969-96130616 | Common:5; Rare:213 | ||||
chr10:96586806-96587200 | Common:5; Rare:157 | ||||
chr10:96831974-96832310 | Rare:128 | ||||
chr10:96833252-96833314 | Rare:23 |