chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087100470871005GA30GENIChomozygous52199900
107087252670872527G-8GENICheterozygous51689606
107087439870874399CA21GENIChomozygous51689612
107087473370874734CA15GENIChomozygous52199902
107087280470872805AG31GENIChomozygous51489542
107087387570873876AG13GENIChomozygous51489543
107087387870873879TC14GENIChomozygous51489544
107087497670874977AG15GENIChomozygous51489546
107087519270875193T-15GENIChomozygous52199904
107087553470875538GTGT----7GENICheterozygous51489551
107087616670876167GA26GENIChomozygous51689620
107087630770876308AG21GENIChomozygous51489555
107087637770876378CCAGG29GENIChomozygous51489556
107087658870876589TA18GENIChomozygous51489557
107087679170876792AAG22GENIChomozygous51489558
107087727970877280GA22GENIChomozygous51489559
107087770770877708AT21GENIChomozygous51689624
107087813070878131AATTCT6GENIChomozygous51489563
107087813470878135TA23GENICheterozygous52199906
107087824670878247CT26GENIChomozygous52160621
107087899270878993GT19GENIChomozygous52160622
107088016170880162AG8GENIChomozygous51489567
107088152770881528GA17GENIChomozygous52160623
107088175670881757AG20GENIChomozygous52160624
107088263970882640GA13GENIChomozygous52160625
107088297670882977GA17GENIChomozygous52160626
107088349970883501AA--13GENICheterozygous51689632
107088350270883503TA13GENICheterozygous52160627
107088531070885311TC11GENIChomozygous51689636
107088584370885850TTGTGTC-------11GENICheterozygous51489574
107088584370885844TTG15GENICheterozygous51489575
107088584370885844TTC15GENICheterozygous51489576
107088584470885845T-11GENICheterozygous51689638