Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:2751655-2751893 | Common:1; Rare:76 | ||||
chr5:6378134-6378365 | Common:1; Rare:59 | ||||
chr5:6378458-6378675 | Rare:88 | ||||
chr5:6632996-6633460 | Common:8; Rare:151; Clinvar:9; Clinvar (benign):4 | ||||
chr5:7868991-7869220 | Common:2; Rare:118; Clinvar (benign):1 | ||||
chr5:9546061-9546375 | Common:7; Rare:73 | ||||
chr5:10249860-10250359 | Common:19; Rare:241; Clinvar:4; Clinvar (benign):2 | ||||
chr5:10353570-10353925 | Common:3; Rare:136 | ||||
chr5:10761083-10761434 | Common:13; Rare:115 | ||||
chr5:14143118-14143373 | Rare:82 | ||||
chr5:14664544-14664718 | Common:3; Rare:82 | ||||
chr5:14871654-14871805 | Rare:41; Clinvar (benign):1 | ||||
chr5:16465718-16465898 | Rare:32 | ||||
chr5:16936045-16936070 | Rare:5 | ||||
chr5:31532032-31532469 | Common:5; Rare:130 |