chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141894409141894430TTTTTTTTTTTTTTTTTTTTT---------------------28GENICheterozygous55017337
7141894426141894430TTTT----28GENICheterozygous55017339
7141894429141894430TTAA30GENICheterozygous55017341
7141894455141894456T-28GENICheterozygous54159988
7141894589141894590CCA28GENICheterozygous54159995
7141894592141894593C-30GENICheterozygous54159996
7141894621141894622AATTGT20GENICheterozygous54160000
7141896965141896966GA32GENIChomozygous54839177
7141897263141897264TTA27GENIChomozygous54160021
7141897299141897300TG22GENIChomozygous54160022
7141898147141898148TA38GENIChomozygous54839180
7141898357141898358AC20GENIChomozygous54839182
7141899795141899796AG39GENIChomozygous54160024
7141900086141900087CT30GENIChomozygous54160025
7141901732141901733CG18GENIChomozygous54160027
7141901745141901746CT18GENIChomozygous54839184
7141902234141902235TTACATACATACATACATAC17GENIChomozygous55017343
7141902956141902957CT40GENIChomozygous54839192
7141903441141903442GGA16GENICpossibly homozygous54160035
7141904704141904705TC28GENIChomozygous54160040
7141906654141906655GGC2GENIChomozygous55032294
7141907488141907489GGTTT12GENICheterozygous55017345
7141907854141907855GA36GENIChomozygous54160046
7141909490141909491CT28GENIChomozygous54839194
7141911360141911361CT30GENIChomozygous54839196
7141911569141911572AGA---31GENIChomozygous54160052
7141911644141911645G-28GENIChomozygous54160054
7141911651141911652G-28GENIChomozygous54160055