chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215148109215160ACACACACACAC------------4GENIChomozygous695734988
6109215292109215293AG48GENIChomozygous534109561
6109215591109215592GGT46GENIChomozygous695734989
6109215956109215957CT57GENICpossibly homozygous534109562
6109216387109216389GT--36GENIChomozygous695734990
6109217437109217438GA41GENIChomozygous534109563
6109217869109217870CCTT9GENIChomozygous695734992
6109218078109218079TG47GENICpossibly homozygous536971571
6109218533109218534TC53GENIChomozygous534109564
6109219610109219611T-14GENIChomozygous695734993
6109219644109219645CG12GENIChomozygous536971572
6109219668109219669TC8GENIChomozygous536971573
6109220171109220172AG32GENICpossibly homozygous534109565
6109220957109220958T-20GENICheterozygous695734994
6109220959109220971TATACATGTTAT------------23GENICpossibly homozygous695734995
6109221202109221203AATTTTT3GENIChomozygous695734996
6109221479109221480AG50GENIChomozygous534109566
6109224345109224346CCTTT3GENICheterozygous695734998
6109224345109224346CCTT3GENICheterozygous695734999
6109224503109224504CT25GENICpossibly homozygous534109567
6109225632109225633TC66GENIChomozygous534109568
6109225969109225970GC72GENICpossibly homozygous534109569
6109226303109226304G-39GENIChomozygous695735000
6109226595109226596GA51GENIChomozygous534109570
6109226868109226869CCT30GENIChomozygous695735001
6109227067109227069GA--23GENICheterozygous695735003
6109227093109227094CCAG15GENICheterozygous695735004
6109227136109227137AG27GENICpossibly homozygous534109571
6109227294109227295TTTTG22GENICheterozygous695735005
6109227301109227302C-25GENICheterozygous695735006
6109227301109227302CCTGTT13GENIChomozygous695735007
6109227305109227306TTC27GENICheterozygous695735008
6109227384109227385TC34GENICpossibly homozygous534109572
6109227502109227503GA59GENIChomozygous534109573
6109227690109227691AT53GENIChomozygous534109574
6109227989109227990AG49GENIChomozygous534109575