chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137872455278724553AG19GENIChomozygous114401806
137872556078725561GA27GENICpossibly homozygous118527510
137873615378736154AG17GENIChomozygous114401814
137874388078743881AG15GENIChomozygous114689341
137874615978746160CA14GENIChomozygous114689342
137874885878748859TA15GENIChomozygous114689343
137875028678750287GA20GENIChomozygous114689344
137875394478753945AG26GENIChomozygous114401820
137876084678760847CT18GENIChomozygous114689345
137876088778760888GA21GENIChomozygous114689346
137876272678762727TC14GENICheterozygous118527518
137877306678773067AG16GENIChomozygous114401856
137877308378773084CT23GENIChomozygous114401858
137877374578773746AG18GENIChomozygous114401862
137877377578773776AG16GENIChomozygous114401864
137877587978775880CT8GENIChomozygous114401874
137877632978776330GA21GENIChomozygous114401878
137878007778780078CT22GENIChomozygous114689347
137878052478780525TA15GENICpossibly homozygous114401890
137878059978780600TC16GENIChomozygous114401892
137878179078781791GA12GENIChomozygous114689348
137878198978781990AG16GENIChomozygous114401896
137878323578783236TA27GENICpossibly homozygous118527520
137878404378784044CA16GENIChomozygous114689349
137878862378788624GA19GENIChomozygous114401924