chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215292109215293AG10GENICheterozygous579304084
6109215591109215592GGT13GENIChomozygous717700247
6109215956109215957CT21GENIChomozygous579304085
6109216387109216389GT--18GENICpossibly homozygous717700248
6109217437109217438GA23GENICpossibly homozygous579304086
6109218078109218079TG1GENIChomozygous581314108
6109218533109218534TC15GENICpossibly homozygous579304087
6109219644109219645CG2GENIChomozygous581314109
6109219668109219669TC2GENIChomozygous581314110
6109219684109219685GGTCGTTTGGTCAGTTTC1GENIChomozygous717700249
6109220171109220172AG12GENICpossibly homozygous579304088
6109220957109220958T-6GENIChomozygous717700251
6109220959109220971TATACATGTTAT------------8GENIChomozygous717700252
6109221479109221480AG12GENIChomozygous579304089
6109224503109224504CT2GENIChomozygous579304090
6109225632109225633TC16GENIChomozygous579304091
6109225969109225970GC10GENICpossibly homozygous579304092
6109226303109226304G-14GENIChomozygous717700253
6109226595109226596GA23GENICpossibly homozygous579304093
6109226868109226869CCT8GENICheterozygous717700255
6109226869109226870T-8GENICheterozygous717700254
6109227291109227292CCTGTTT4GENIChomozygous717700256
6109227384109227385TC11GENICheterozygous579304094
6109227502109227503GA13GENIChomozygous579304095
6109227690109227691AT13GENIChomozygous579304096
6109227989109227990AG10GENICpossibly homozygous579304097