chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186165780861657809TA4GENIChomozygous110372385
186165986961659870TG58GENIChomozygous110372387
186166183561661836GA43GENIChomozygous110372389
186166219661662197TA37GENIChomozygous110372391
186166269761662698TC58GENIChomozygous110372393
186166420461664205TC25GENICheterozygous110372395
186166449361664494AG58GENIChomozygous110372397
186166530861665309TA37GENIChomozygous110372399
186166561561665616GC51GENIChomozygous110372401
186166578861665789TC51GENIChomozygous110372403
186166602861666029AT47GENIChomozygous110372405
186166615461666155TC47GENIChomozygous110372407
186166637761666378TC44GENIChomozygous110372409
186166754361667544TC33GENIChomozygous110372411
186166815461668155CT43GENIChomozygous110372413
186166880261668803TC20GENICpossibly homozygous110372415
186167019861670199CT48GENIChomozygous110372417
186167053761670538TG45GENIChomozygous110372419
186167054161670542GT45GENIChomozygous110372421
186167080361670804AC47GENIChomozygous110372423
186167082861670829GA58GENIChomozygous110372425
186167199661671997TG23GENIChomozygous110372427
186167237161672372TC36GENIChomozygous110372429
186167263761672638AG44GENIChomozygous110372431