Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70354656-70354856 | Rare:68 | ||||
chr1:70411053-70411297 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080984-71081383 | Rare:108 | ||||
chr1:74198148-74198331 | Common:2; Rare:107 | ||||
chr1:75724284-75724598 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):3 | ||||
chr1:75724601-75724778 | Common:2; Rare:89; Clinvar:5; Clinvar (benign):2 | ||||
chr1:76074519-76074767 | Common:2; Rare:99 | ||||
chr1:77219407-77219507 | Rare:42 | ||||
chr1:77683360-77683583 | Common:1; Rare:73 | ||||
chr1:77759673-77759946 | Common:2; Rare:110 | ||||
chr1:77888436-77888600 | Common:1; Rare:33 | ||||
chr1:77888604-77888688 | Rare:23; Clinvar:1 | ||||
chr1:77979034-77979275 | Common:2; Rare:80 | ||||
chr1:78004552-78004873 | Common:3; Rare:80 | ||||
chr1:81800059-81800386 | Common:2; Rare:86 |