chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12830297928302980CA14GENIChomozygous109067772
12831071928310720TC7GENIChomozygous120478717
12831072028310721CT8GENIChomozygous120552992
12831573928315740AG15GENIChomozygous109067774
12831869528318696TC14GENIChomozygous109067776
12831635828316359CA13GENIChomozygous108065806
12831636428316365GT10GENIChomozygous108065807
12832101228321013CT14GENICheterozygous108701278
12832588028325881TC12GENIChomozygous108701282
12833176128331762TC9GENIChomozygous108701290
12833338528333386CT9GENICheterozygous120658059
12833807928338080GA11GENIChomozygous108701293
12834784728347848CA4GENIChomozygous108701325
12835073428350735AG7GENIChomozygous108701342
12835129328351294CT5GENIChomozygous108701344
12836030928360310TC24GENIChomozygous108701373
12836303628363037AC24GENIChomozygous108701379
12836591428365915AG13GENIChomozygous109067784
12837044528370446AG10GENIChomozygous109067786
12837136728371368AG14GENIChomozygous108701392
12837302628373027TC17GENIChomozygous109067788
12837528228375283CT17GENIChomozygous109067790
12837700928377010CT6GENIChomozygous108701404
12837905128379052GA18GENIChomozygous109067792
12838043828380439TC7GENICheterozygous108701405
12838109528381096GA20GENIChomozygous109067794
12838169528381696TC14GENIChomozygous109067796
12838302828383029GC18GENIChomozygous109067798
12838534128385342GA11GENIChomozygous109067800
12838614728386148GA11GENIChomozygous109067802
12839127228391273TC13GENIChomozygous108701426
12832004428320045CT4GENICheterozygous125354873
12833517028335171GT5GENICheterozygous125354875
12834762828347629CT5GENICheterozygous125354877
12838801828388019TC10GENICheterozygous125354880