chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122632262726322628CCTT15GENIChomozygous50147537
122632268626322687AT25GENIChomozygous50147542
122632326526323266G-20GENIChomozygous50147548
122632340726323408GGTTTTTTTTTTTTTTGTTTTTGTTTTTT9GENIChomozygous50557816
122632397026323971TC26GENIChomozygous50147550
122632428526324286CT33GENIChomozygous50147552
122632430726324308CT32GENIChomozygous50405082
122632540326325404CG30GENIChomozygous50147554
122632563126325634TTT---2GENIChomozygous50539332
122632361326323614CT28GENIChomozygous50485094
122632553326325534CCT5GENICheterozygous50597929
122632622526326226TC28GENIChomozygous50147558
122632635826326359TA33GENIChomozygous50405086
122632641526326416AG30GENIChomozygous50147560
122632661826326619CA39GENIChomozygous50485096
122632690526326906AC29GENIChomozygous50147562
122632859626328597GT30GENICpossibly homozygous50147564
122632944026329441TC34GENIChomozygous50147566
122632963526329637TT--23GENICheterozygous50826681
122632963626329637T-23GENICpossibly homozygous50539333
122633059826330599CT30GENIChomozygous50405090
122633317126333172CT24GENIChomozygous50147570
122633345326333454GA18GENIChomozygous50147572
122633361626333617CA25GENIChomozygous50405092
122633416726334168TC16GENIChomozygous50147576
122633482526334826CA34GENIChomozygous50147578
122633520126335202TTTG8GENICheterozygous50539334
122633601726336018TTACAC24GENIChomozygous50147580
122633733926337340AAGCCT7GENIChomozygous50485098