chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104383396143833962GT14GENIChomozygous51436667
104383693943836940A-5GENIChomozygous51436673
104383706343837064CCGT1GENIChomozygous51871717
104383866743838668CG16GENIChomozygous51436677
104384069243840693CT19GENIChomozygous52048636
104384075143840752TTATA13GENIChomozygous52048638
104384112943841130AC11GENIChomozygous52048642
104384119343841195TG--13GENIChomozygous51436680
104384135243841353TC9GENIChomozygous52148520
104383839743838398CT12GENIChomozygous52148514
104384031043840311GGT13GENIChomozygous52148516
104384106943841070TA8GENIChomozygous52148518
104384118143841182AT14GENIChomozygous52839510
104384118243841183TG14GENIChomozygous52839513
104384181443841815TC9GENIChomozygous51436681
104384183843841839TC13GENIChomozygous51436682
104384186543841866T-15GENIChomozygous52048646
104384227543842276CT18GENIChomozygous52048648
104384227643842277AG18GENIChomozygous51436683
104384234843842349TG16GENIChomozygous52048650
104384434143844342T-5GENICheterozygous52048652
104384434843844349TTC6GENICheterozygous52839515
104384449043844491CCATTAACTATGTAAT6GENIChomozygous52048654
104384498343844984AG10GENIChomozygous52048658
104384516443845165TC16GENIChomozygous51436685
104384547543845476GA10GENICpossibly homozygous52148522
104384744043847441CA10GENIChomozygous52048660
104384831043848311GT14GENICpossibly homozygous52048662
104384915243849153A-8GENICheterozygous52191277
104384979943849800GA7GENIChomozygous52048664
104385038643850387TG13GENIChomozygous51635303
104385038743850388CT13GENIChomozygous52317644
104385161743851618A-6GENIChomozygous52048668
104385254943852550AAAC3GENIChomozygous51436691
104385859843858599AG9GENIChomozygous51436696
104385974143859742T-11GENIChomozygous52148524
104386056943860570AG17GENIChomozygous51436698
104386209043862091AG10GENIChomozygous51436699
104386212543862126AG9GENIChomozygous51436700
104386281343862814GA8GENICheterozygous52191319
104386565643865657GT9GENIChomozygous52148526