chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117514931117514932AC18GENIChomozygous111684554
3117515039117515040CT20GENIChomozygous111684555
3117515460117515461TA27GENIChomozygous111684556
3117515873117515874CT19GENIChomozygous111684559
3117516399117516400CG20GENIChomozygous111684560
3117516672117516673AG29GENIChomozygous112294450
3117516741117516742AG28GENIChomozygous111684563
3117517299117517300AG20GENIChomozygous112294452
3117517453117517454AG20GENIChomozygous112294454
3117517889117517890AG22GENIChomozygous112294456
3117517932117517933AG25GENIChomozygous111684566
3117518096117518097GA22GENIChomozygous112294458
3117518575117518576CT19GENIChomozygous112294460
3117518745117518746AG22GENIChomozygous111684567
3117518793117518794AC18GENIChomozygous112294462
3117518902117518903GC23GENIChomozygous112294464
3117519063117519064CT33GENIChomozygous111684568
3117519915117519916TG5GENIChomozygous112294468
3117520083117520084GA16GENIChomozygous112294470
3117520127117520128AG16GENIChomozygous111684570
3117520611117520612GT19GENIChomozygous112294478
3117521823117521824AG19GENIChomozygous112294484
3117521896117521897GT20GENIChomozygous111684574
3117521958117521959TC27GENIChomozygous112020845
3117521962117521963TC26GENIChomozygous112294486
3117522081117522082CT25GENIChomozygous112294488
3117522183117522184TC30GENIChomozygous112294490
3117522443117522444AG14GENIChomozygous112294492
3117522628117522629TC15GENIChomozygous111684575
3117522786117522787GC23GENIChomozygous111684576
3117523453117523454GA30GENIChomozygous111684577
3117523821117523822AG19GENIChomozygous112294498
3117523866117523867AG27GENIChomozygous111684579
3117524461117524462TC12GENIChomozygous111684580
3117524586117524587TC22GENIChomozygous112294500
3117525045117525046AG20GENIChomozygous111684581