chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42778672927786729GTGCTTGCTAGGCAA36GENIChomozygous128017626
42778673327786733TCTA27GENIChomozygous128017627
42778673527786735ACT27GENIChomozygous128017628
42778673627786737GA23GENIChomozygous122014859
42779067227790673TG51GENIChomozygous112565504
42782631927826319TCTTGGTCAGGCCCATGTTG51GENIChomozygous128017629
42783154527831546TC20GENIChomozygous112565508
42783159127831591A23GENIChomozygous128017630
42783258727832587C3GENIChomozygous128017631
42783539327835393T6GENIChomozygous128017632
42783542127835421T8GENIChomozygous128017633
42783543027835431T9GENIChomozygous128017634
42783543827835439TG10GENIChomozygous112565510
42783544327835443T10GENIChomozygous128017635
42783545627835457G13GENIChomozygous128017636
42783545827835459A13GENIChomozygous128017637
42784536027845361C27GENICheterozygous128017638
42786188927861890GT50GENICheterozygous113256102
42786191127861912GT52GENICheterozygous113256103
42792520527925206T6GENIChomozygous128017641
42792523627925238TA10GENIChomozygous128017642
42792523927925239TCA10GENIChomozygous128017643
42792529127925292AC19GENIChomozygous112565518
42792530427925304C20GENIChomozygous128017644
42792533327925334C19GENIChomozygous128017645
42792533727925337A19GENIChomozygous128017646
42792534227925343C19GENIChomozygous128017647
42792535427925356GT20GENIChomozygous128017648
42792536127925361T18GENIChomozygous128017649
42779856427798566TC30GENICheterozygous133543688
42793768827937690CT17GENICheterozygous130648196
42782398027823981T22GENICheterozygous130294151
42786471027864711G26GENICheterozygous132055841
42790049927900500A41GENICheterozygous132964095