chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706738747067388TC26GENIChomozygous976552609
104706850747068508AG21GENIChomozygous976552610
104708237347082374GA23GENIChomozygous976552611
104708308147083082GA18GENIChomozygous976552612
104708367247083673TC25GENIChomozygous976552613
104708432247084323AG25GENIChomozygous976552614
104708446147084462TC21GENIChomozygous976552615
104708642247086423GC35GENIChomozygous976552616
104708650047086501AG26GENIChomozygous976552617
104708665247086653CA31GENIChomozygous976552618
104708734847087349GA35GENIChomozygous976552619
104708763947087640CT14GENIChomozygous976552620
104708819347088194GT23GENIChomozygous976552621
104708909147089092GT25GENIChomozygous976552622
104708996147089962TC16GENIChomozygous976552623
104709009547090096TA10GENIChomozygous976552624
104709123347091234GA29GENIChomozygous976552625
104709128847091289GT20GENIChomozygous976552626
104709153347091534CT26GENIChomozygous976552627
104709296347092964TC21GENIChomozygous976552628
104709370847093709TC30GENIChomozygous976552629
104709390547093906TA24GENIChomozygous976552630
104709401947094020TC23GENIChomozygous976552631
104709540047095401AC14GENIChomozygous976552632
104709698847096989CT17GENIChomozygous976552633
104709700447097005TC15GENIChomozygous976552634
104709781247097813TC17GENIChomozygous976552635
104709839847098399CT21GENIChomozygous976552636
104710175847101759CT18GENIChomozygous976552637