chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161909741119097412GA14GENIChomozygous939439353
161909779819097799CT19GENIChomozygous939439354
161909817519098176GT26GENIChomozygous939439355
161909930319099304TA30GENIChomozygous939439356
161909955919099560AG21GENIChomozygous939439357
161909977219099773TC10GENIChomozygous939439358
161909983319099834TC20GENIChomozygous939439359
161910008019100081CT23GENIChomozygous939439360
161910008119100082AG23GENIChomozygous939439361
161910079419100795AT23GENIChomozygous939439362
161910166819101669CT18GENIChomozygous939439363
161910184519101846TC16GENIChomozygous939439364
161910344019103441CA19GENIChomozygous939439365
161910448719104488CT26GENIChomozygous939439366
161910478119104782TC16GENIChomozygous939439367
161910500219105003AG31GENIChomozygous939439368
161911347419113475CT14GENIChomozygous939439369
161911393319113934CT19GENIChomozygous939439370
161911411919114120CT20GENIChomozygous939439371
161911547419115475TC21GENIChomozygous939439372
161911582819115829GA22GENIChomozygous939439373
161911794119117942CT25GENIChomozygous939439374
161911794219117943CT24GENIChomozygous939439375
161911846619118467GA25GENIChomozygous939439376
161911933219119333CT7GENIChomozygous939439377
161911958419119585AC29GENIChomozygous939439378
161911986819119869TC19GENIChomozygous939439379
161912032919120330AG18GENIChomozygous939439380
161912091319120914CT16GENIChomozygous939439381
161912153419121535CA8GENIChomozygous939439382
161912292119122922TC17GENIChomozygous939439383
161912367519123676AC18GENIChomozygous939439384