chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
93953387939533880CT5GENICheterozygous117325701
93963628639636287TC9GENIChomozygous117792945
93963696739636968CG18GENIChomozygous117325884
93963697739636978CG21GENIChomozygous117325885
93971393639713937CT28GENIChomozygous117326082
93974555739745558TA22GENIChomozygous117326233
93979307939793080GT23GENIChomozygous117805467
93979810539798106GT12GENICheterozygous120410733
93980733839807339AG31GENIChomozygous117326571
93981256839812569AC24GENIChomozygous117530471
93981258839812589GA22GENIChomozygous117326619
93981317339813174AG29GENIChomozygous120410734
93981348139813482CG23GENIChomozygous117530493
93987524239875243TC32GENIChomozygous120410735
93988773939887740GA32GENIChomozygous117706317
93991788639917887TG21GENIChomozygous117326895
93991791339917914TG23GENIChomozygous117326896
93994257939942580GC28GENIChomozygous117326943
93994280239942803GT33GENIChomozygous117531033
93994344039943441CG12GENIChomozygous117326945
93997592539975926AC31GENIChomozygous117531368
93997597639975977AC34GENIChomozygous117531370
93997597739975978CT34GENIChomozygous117531372
93997627739976278GC17GENIChomozygous117706321
93999074239990743TA33GENIChomozygous117327166