chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123563225123563226TC9GENIChomozygous116082376
7123563269123563270TC12GENIChomozygous116082377
7123563330123563331TC28GENIChomozygous116082378
7123563539123563540CT26GENIChomozygous116082379
7123563553123563554CT23GENIChomozygous116082380
7123563753123563754GC27GENIChomozygous116082381
7123564100123564100A28GENIChomozygous132657714
7123564126123564127GA29GENIChomozygous116082382
7123564226123564227CT21GENIChomozygous116082383
7123564228123564229CA21GENIChomozygous116082384
7123564602123564603CT21GENIChomozygous116082385
7123564701123564702AG27GENIChomozygous116082386
7123564883123564884TC22GENIChomozygous116082387
7123564928123564929AT20GENIChomozygous116082388
7123564937123564938GT19GENIChomozygous116082389
7123564994123564995AG23GENIChomozygous116082390
7123565121123565122GA25GENIChomozygous116082391
7123565333123565334TC29GENIChomozygous116082392
7123566518123566519AG25GENIChomozygous116082393
7123566529123566530CT24GENIChomozygous116082394
7123566854123566855CT25GENIChomozygous116082395
7123566877123566877C22GENIChomozygous132657715
7123567200123567201CT22GENIChomozygous116082396
7123567709123567710TC22GENIChomozygous116082397
7123569231123569232AG16GENIChomozygous116082398
7123570079123570080CT15GENIChomozygous116082399
7123570480123570481TC15GENIChomozygous116082400
7123570535123570536GA14GENIChomozygous116082401
7123571603123571603AAAC12GENICpossibly homozygous128513976
7123571632123571633GA15GENICpossibly homozygous115863644
7123568207123568208TC24GENIChomozygous115863640