chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85399005953990060AG13GENIChomozygous67997600
85399047553990476CT19GENIChomozygous67997603
85399090253990903TC9GENIChomozygous68733184
85399135053991350A17GENICheterozygous69833699
85399187953991880GC24GENIChomozygous67997606
85399200353992004TA25GENIChomozygous67997610
85399220053992201TC24GENIChomozygous67997613
85399360653993607AG12GENIChomozygous67997620
85399420953994210CT15GENIChomozygous67997624
85399422953994231CC4GENIChomozygous69398558
85399475453994755TC14GENIChomozygous67997627
85399959353999594AC10GENIChomozygous67997630
85400030354000304CT6GENIChomozygous67997633
85400036554000366GT5GENIChomozygous67997648
85400038054000381C5GENIChomozygous69398559
85400039354000394TC14GENIChomozygous67997652
85400076754000767T14GENICheterozygous69833701
85400078754000787T13GENIChomozygous69833703
85400082654000827CT14GENIChomozygous69398562
85400082754000828TC14GENIChomozygous69398563
85400087754000878G5GENIChomozygous69833705
85400181754001818GA27GENIChomozygous67997658
85400192754001928GT21GENIChomozygous67997661
85400278354002784CG12GENIChomozygous67997665
85400392454003925TA23GENIChomozygous67997669
85400659554006596CT13GENIChomozygous67997680
85400816854008169AT31GENIChomozygous67997683
85400886354008864GA30GENIChomozygous67997689
85400987354009874AT4GENIChomozygous67997692
85401001254010013GA19GENIChomozygous67997695
85401150454011506GT15GENICheterozygous69833707
85401150554011506TG6GENIChomozygous69277702