chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154880731748807318AG19GENIChomozygous112503477
154880748348807484CT5GENICheterozygous112503479
154880919848809199CA11GENIChomozygous125777504
154880968248809683GT10GENICheterozygous118916577
154881076848810769GA14GENIChomozygous112503485
154881182848811829TC18GENIChomozygous112503487
154881201548812016GT19GENIChomozygous112503489
154881271348812714AC21GENIChomozygous112503491
154881291148812912TC12GENIChomozygous112503493
154881300648813007GA11GENIChomozygous112503495
154881324848813249TC22GENIChomozygous112503497
154881388648813887AG18GENIChomozygous112503499
154881397148813972AG12GENIChomozygous112503501
154881426648814267CT26GENIChomozygous112503503
154881439748814398GA13GENIChomozygous112503505
154881474548814746GA9GENIChomozygous112503509
154881510148815102GA7GENICheterozygous125855854
154881519748815198AG11GENIChomozygous125777505
154881557248815573CT22GENIChomozygous112503515
154881589248815893CG19GENIChomozygous112503517
154881596348815964TC6GENIChomozygous112503519
154881597348815974GC9GENIChomozygous112503521
154881599148815992GA10GENIChomozygous112503524
154881658548816586CT17GENIChomozygous112503526
154881668248816683GA19GENIChomozygous112503528
154881681748816818AG15GENICheterozygous112503530
154881734948817350TC23GENIChomozygous112503532
154881832248818323CA13GENIChomozygous112503534
154881865748818658AG13GENIChomozygous112503536
154881907548819076AG18GENIChomozygous112503538
154881949148819492AG13GENIChomozygous112503540
154881953948819540AG5GENIChomozygous112503542
154881969448819695TC28GENIChomozygous112809050
154882253148822532AG11GENIChomozygous112809052
154882333048823331AG11GENIChomozygous112503544
154882373648823737GA21GENIChomozygous112503546
154883080248830803AC17GENIChomozygous112503552