Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5610904-5611154 | Common:2; Rare:88 | ||||
chr20:5950391-5950720 | Common:8; Rare:101 | ||||
chr20:6053933-6054358 | Common:2; Rare:70 | ||||
chr20:6123397-6123468 | Common:3; Rare:10; Clinvar:4; Clinvar (benign):2 | ||||
chr20:13784865-13785080 | Common:2; Rare:94; Clinvar (benign):3 | ||||
chr20:16573293-16573543 | Common:1; Rare:71 | ||||
chr20:16729878-16730073 | Rare:61 | ||||
chr20:17569990-17570210 | Common:3; Rare:96 | ||||
chr20:17968436-17968594 | Common:4; Rare:66 | ||||
chr20:17968773-17969129 | Common:4; Rare:126 | ||||
chr20:18137744-18137952 | Common:1; Rare:77 | ||||
chr20:18467136-18467448 | Common:1; Rare:64 | ||||
chr20:18497165-18497308 | Common:1; Rare:54 | ||||
chr20:18507464-18507641 | Rare:46; Clinvar:1 | ||||
chr20:18507785-18507972 | Common:2; Rare:58; Clinvar:5; Clinvar (benign):2 |