chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132682879926828800TC33GENIChomozygous114302992
132683075026830751AG20GENIChomozygous114302993
132683219026832191GA36GENIChomozygous114516502
132683240426832405GT17GENIChomozygous114302994
132683337026833371AT30GENIChomozygous114302996
132683582726835828TC26GENIChomozygous114302998
132683797726837978GA25GENIChomozygous114516504
132683823726838238CT20GENIChomozygous114516506
132683828626838287CT29GENIChomozygous114516508
132683840226838403GA28GENIChomozygous114516510
132683841726838418GC31GENIChomozygous114516512
132683877826838779AG22GENIChomozygous114516514
132683899826838999AG28GENIChomozygous114303002
132683914826839149GA32GENIChomozygous114516516
132683971526839716TC39GENIChomozygous114516518
132683975026839751TC43GENIChomozygous114516520
132683980126839802GC46GENIChomozygous114516522
132684049826840499GA28GENICpossibly homozygous114516524
132684195526841956GA21GENIChomozygous114516526
132684446026844461AG28GENIChomozygous114516528
132684538326845384CA13GENIChomozygous114303020
132684579026845791AG12GENIChomozygous114303021
132684613126846132CA25GENIChomozygous114303023