chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141894409141894430TTTTTTTTTTTTTTTTTTTTT---------------------25GENICpossibly homozygous55017337
7141894426141894430TTTT----25GENICheterozygous55017339
7141894429141894430TTAA21GENICpossibly homozygous55017341
7141894455141894456T-36GENICheterozygous54159988
7141894589141894590CCA19GENICheterozygous54159995
7141894592141894593C-19GENICheterozygous54159996
7141894621141894622AATTGT25GENICheterozygous54160000
7141895881141895882CT6GENICheterozygous54160019
7141895898141895899CCCCT6GENICheterozygous55145693
7141896965141896966GA16GENIChomozygous54839177
7141897263141897264TTA22GENIChomozygous54160021
7141897299141897300TG32GENICpossibly homozygous54160022
7141898147141898148TA27GENIChomozygous54839180
7141898357141898358AC17GENIChomozygous54839182
7141899795141899796AG35GENIChomozygous54160024
7141900086141900087CT29GENIChomozygous54160025
7141901732141901733CG20GENIChomozygous54160027
7141901745141901746CT16GENIChomozygous54839184
7141902234141902235TTACATACATACATACATAC19GENICheterozygous55017343
7141902956141902957CT26GENIChomozygous54839192
7141903441141903442GGA18GENICpossibly homozygous54160035
7141904704141904705TC28GENIChomozygous54160040
7141906654141906655GGC5GENIChomozygous55032294
7141907488141907489GGTTT12GENICheterozygous55017345
7141907854141907855GA26GENIChomozygous54160046
7141909490141909491CT31GENIChomozygous54839194
7141911569141911572AGA---23GENIChomozygous54160052
7141911644141911645G-16GENIChomozygous54160054
7141911651141911652G-18GENIChomozygous54160055