chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123563330123563331TC6GENIChomozygous116082378
7123563539123563540CT9GENIChomozygous116082379
7123563553123563554CT9GENIChomozygous116082380
7123563753123563754GC16GENIChomozygous116082381
7123564126123564127GA20GENIChomozygous116082382
7123564226123564227CT7GENIChomozygous116082383
7123564228123564229CA8GENIChomozygous116082384
7123564602123564603CT18GENICpossibly homozygous116082385
7123564701123564702AG21GENIChomozygous116082386
7123564883123564884TC16GENIChomozygous116082387
7123564928123564929AT10GENIChomozygous116082388
7123564937123564938GT8GENIChomozygous116082389
7123564994123564995AG11GENIChomozygous116082390
7123565121123565122GA20GENIChomozygous116082391
7123565333123565334TC27GENIChomozygous116082392
7123566518123566519AG14GENIChomozygous116082393
7123566529123566530CT15GENIChomozygous116082394
7123567709123567710TC15GENIChomozygous116082397
7123568207123568208TC26GENIChomozygous115863640
7123569231123569232AG7GENIChomozygous116082398
7123570079123570080CT23GENIChomozygous116082399
7123570480123570481TC5GENIChomozygous116082400
7123570535123570536GA22GENIChomozygous116082401
7123571632123571633GA16GENICheterozygous115863644