chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103634601736346018AG2GENIChomozygous116560537
103634605136346052TC3GENIChomozygous116560539
103634677736346778TG6GENIChomozygous116560549
103634759836347599AG5GENIChomozygous116560551
103634807036348071CT4GENIChomozygous116560553
103634890036348901AG5GENIChomozygous116758979
103634892636348927GA5GENIChomozygous116560555
103635110336351104CT6GENIChomozygous116560557
103635115936351160CT8GENIChomozygous116560559
103635120536351206AG10GENIChomozygous116560561
103635121236351213AG9GENIChomozygous116560563
103635121636351217CT9GENIChomozygous116560565
103635123336351234CT8GENIChomozygous116560567
103635199836351999TC5GENICheterozygous117409494
103635202336352024GA4GENICheterozygous117409496
103635203136352032GA4GENICheterozygous117409498
103635558436355585TC2GENIChomozygous116868225
103635569536355696TC11GENIChomozygous116560575
103635791736357918AT13GENIChomozygous116560581
103635806036358061AG4GENIChomozygous116759045
103635847136358472CT3GENIChomozygous116560583
103635886836358869CT3GENIChomozygous116560585
103635949936359500CT10GENIChomozygous116560587
103635982136359822AG5GENIChomozygous117177868
103635982436359825AG5GENIChomozygous117177869
103636004236360043CT6GENIChomozygous116868227
103636053136360532TG6GENIChomozygous116868229
103636093636360937TC8GENIChomozygous116868231
103636132036361321CT3GENIChomozygous116560595
103636152436361525GC2GENIChomozygous116868233
103636152736361528GA2GENIChomozygous116560599
103636161036361611TC6GENIChomozygous116868235
103636218336362184GA2GENIChomozygous116868237
103636308336363084GA4GENIChomozygous116868239
103636313336363134AG5GENIChomozygous116560613