chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99851529098515291TC7GENIChomozygous1001054280
99851555498515555AG6GENIChomozygous1001054281
99851563598515636TC7GENIChomozygous1001054282
99851593698515937TC4GENIChomozygous1001054283
99851596098515961TC8GENIChomozygous1001054284
99851818998518190GA3GENIChomozygous1001054285
99851854298518543AC4GENICheterozygous1001054286
99851915298519153AG6GENIChomozygous1001054287
99851974198519742CT4GENIChomozygous1001054288
99851983498519835TC6GENIChomozygous1001054289
99852311498523115AT7GENIChomozygous1001054290
99852480998524810TC10GENIChomozygous1001054291
99852518698525187GA4GENIChomozygous1001054292
99852731698527317AC6GENIChomozygous1001054293
99852795598527956CT5GENIChomozygous1001054294
99852795798527958CT5GENIChomozygous1001054295
99852795898527959AG5GENIChomozygous1001054296
99852900398529004GA7GENIChomozygous1001054297
99852947898529479GA10GENIChomozygous1001054298
99853040698530407GA10GENIChomozygous1001054299
99853122498531225CA7GENIChomozygous1001054300
99853145698531457AG8GENIChomozygous1001054301
99853147998531480GA9GENIChomozygous1001054302
99853210398532104CT8GENIChomozygous1001054303
99853317598533176AG5GENIChomozygous1001054304
99853336598533366TA11GENIChomozygous1001054305
99853439798534398GA9GENIChomozygous1001054306
99853595998535960GA7GENIChomozygous1001054307