chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85329918353299183T1GENIChomozygous130362395
85329977153299772TC21GENIChomozygous116820420
85330050953300510GA22GENIChomozygous116820422
85330066953300669CCC13GENIChomozygous131047582
85330174153301742TC24GENIChomozygous116820424
85330316553303166GA21GENIChomozygous116820426
85330377453303775GA27GENIChomozygous116820428
85330388253303884GC14GENIChomozygous130362396
85330389153303892CT15GENIChomozygous116820430
85330434453304345TC21GENIChomozygous116820432
85330504853305049TC23GENIChomozygous116820434
85330569053305690T17GENIChomozygous130362397
85330655053306551TC21GENIChomozygous116820440
85330708753307088CT16GENIChomozygous116820442
85330806653308067GA23GENIChomozygous116820444
85330901553309017AT24GENIChomozygous130362398
85330977753309778TC13GENIChomozygous116820446
85331164253311643TC33GENIChomozygous117928036
85330978453309785TG13GENIChomozygous116820448
85331055853310559CA20GENIChomozygous116820450
85331101653311017GA16GENIChomozygous116820452
85331164353311644AT34GENIChomozygous117157392
85331213153312132CT11GENIChomozygous116820454
85331243853312439TC19GENIChomozygous116820456
85332833553328336GA24GENIChomozygous116820458
85333208253332082ATTT16GENIChomozygous130362399
85333257153332572T17GENICheterozygous130362400
85334343753343445TTTCTTTA3GENIChomozygous130362401