Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:76756150-76756510 | Common:5; Rare:143 | ||||
chr5:78595081-78595400 | Rare:60 | ||||
chr5:78597082-78597244 | Rare:41 | ||||
chr5:78984480-78985062 | Common:16; Rare:269; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
chr5:79546990-79547280 | Common:5; Rare:103 | ||||
chr5:79547574-79547757 | Common:3; Rare:36 | ||||
chr5:80184401-80184851 | Common:11; Rare:135 | ||||
chr5:83474281-83474743 | Common:6; Rare:157 | ||||
chr5:90899000-90899350 | Common:1; Rare:92 | ||||
chr5:91314358-91314546 | Common:4; Rare:66 | ||||
chr5:92944960-92945410 | Rare:138 | ||||
chr5:92945759-92945889 | Rare:17 | ||||
chr5:93621430-93621760 | Common:6; Rare:149 | ||||
chr5:95759129-95759299 | Rare:67 | ||||
chr5:95823670-95824050 | Rare:199 |