chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106656003966560040CT29GENICheterozygous51908298
106656009066560091TC36GENICheterozygous51908300
106656063566560636CG12GENICheterozygous51908302
106656066166560662AG14GENICheterozygous51908304
106656560366565604GA15GENICheterozygous51908328
106656579166565792TC16GENICheterozygous51908330
106657240266572403GA18GENICheterozygous51908351
106657304466573045CT24GENICheterozygous51908359
106659001866590019AC30GENICheterozygous51908449
106659001966590020AT32GENICheterozygous51908451
106659427466594275AG13GENICheterozygous51908488
106659463366594634TC9GENICheterozygous51908490
106659643766596438TC26GENICheterozygous51908500
106659762466597625TC7GENICheterozygous51908506
106659762566597626GA8GENICheterozygous51908508
106659773266597733TC5GENICheterozygous51908510
106659803066598031AT21GENICheterozygous51908512
106660056566600566TC11GENICheterozygous51908524
106660309866603099TC18GENICheterozygous51908538
106660339466603401TGAGGGA-------13GENICheterozygous51908540
106661464366614644AG17GENICheterozygous51479869
106662226066622261CT13GENICheterozygous51479881
106662533166625332AAAC12GENICheterozygous51908566
106663184866631849CCT35GENICheterozygous51908572