chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85399005953990060AG9GENIChomozygous67997600
85399047553990476CT20GENIChomozygous67997603
85399090253990903TC20GENIChomozygous68733184
85399135053991350A15GENICheterozygous69758808
85399187953991880GC13GENIChomozygous67997606
85399200353992004TA24GENIChomozygous67997610
85399220053992201TC16GENIChomozygous67997613
85399360653993607AG7GENIChomozygous67997620
85399420953994210CT13GENIChomozygous67997624
85399475453994755TC7GENIChomozygous67997627
85400036554000366GT6GENIChomozygous67997648
85400039354000394TC13GENIChomozygous67997652
85400076754000767T11GENICheterozygous69758811
85400078754000787T9GENIChomozygous69758814
85399422953994231CC9GENICheterozygous69398558
85400038054000381C11GENIChomozygous69398559
85400082654000827CT7GENIChomozygous69398562
85400082754000828TC7GENIChomozygous69398563
85400181754001818GA9GENIChomozygous67997658
85400192754001928GT16GENIChomozygous67997661
85400278354002784CG14GENIChomozygous67997665
85400392454003925TA25GENIChomozygous67997669
85400659554006596CT16GENIChomozygous67997680
85400816854008169AT13GENIChomozygous67997683
85400886354008864GA31GENIChomozygous67997689
85400987354009874AT5GENIChomozygous67997692
85401001254010013GA15GENIChomozygous67997695
85401142154011421TG20GENICheterozygous69758817
85401150554011506TG6GENIChomozygous69277702