Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72781831-72782198 | Common:1; Rare:144 | ||||
chr13:75537801-75538170 | Common:3; Rare:118 | ||||
chr13:75549429-75549837 | Common:8; Rare:108 | ||||
chr13:76992018-76992181 | Common:1; Rare:75; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:77918800-77918941 | Common:1; Rare:32 | ||||
chr13:79405785-79405898 | Rare:40 | ||||
chr13:80339300-80339457 | Common:2; Rare:43 | ||||
chr13:93226924-93227089 | Rare:32; Clinvar:1 | ||||
chr13:93227217-93227467 | Common:1; Rare:56; Clinvar:5; Clinvar (benign):1 | ||||
chr13:95676926-95677213 | Common:3; Rare:101 | ||||
chr13:96053374-96053515 | Common:2; Rare:57 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088948-100089117 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596804-102597035 | Common:1; Rare:112 | ||||
chr13:102798950-102799181 | Common:1; Rare:48 |