chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183467992934679930CT7GENICheterozygous148634753
183467992934679930C7GENICheterozygous404406577
183471194434711945A6GENICheterozygous404266018
183471194434711945AT6GENICheterozygous404266019
183471915234719153T19GENIChomozygous403431911
183471915234719153TA19GENICheterozygous403431912
183471915334719154G19GENIChomozygous403431913
183471915334719154GC19GENICheterozygous403431914
183472093934720940AG18GENIChomozygous140296664
183471194034711941A6GENICheterozygous403671852
183471194034711941AT6GENICheterozygous403671853
183471194234711943A6GENICheterozygous403671854
183471194234711943AT6GENICheterozygous403671855
183471915734719158CA20GENIChomozygous140296660
183472091734720918AG20GENIChomozygous140296661
183472092434720925GA20GENIChomozygous140296662
183472093134720932AG19GENIChomozygous140296663
183473195134731952GT24GENIChomozygous140296665
183494160334941604A7GENICheterozygous403431917
183494160334941604AT7GENICheterozygous403431918
183498626034986261GA27GENICheterozygous140296667
183498629634986297AG25GENICheterozygous144193639
183504515435045155CT17GENICpossibly homozygous403431942
183504515435045155C17GENICheterozygous403431943
183504515735045158GA19GENIChomozygous140296670
183504512235045123G16GENICpossibly homozygous141055534
183471915034719154TCTG19GENIChomozygous140218334
183504513435045136TT17GENIChomozygous141055535