chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144820586144820587GA25GENIChomozygous115945946
7144824467144824468TC11GENIChomozygous115945948
7144830091144830092TC21GENIChomozygous115945949
7144830220144830222TT23GENIChomozygous128532105
7144830064144830065TC20GENIChomozygous116378314
7144830096144830097AC20GENIChomozygous115945951
7144831797144831798AC18GENIChomozygous115945952
7144838282144838283GA19GENIChomozygous116378316
7144841028144841030CA20GENIChomozygous128532122
7144844920144844921T9GENIChomozygous128532123
7144844938144844940CC9GENIChomozygous128532124
7144849550144849551CT18GENIChomozygous116378318
7144852139144852140AC30GENIChomozygous116378320
7144856922144856923A18GENIChomozygous128532129
7144860812144860813GA22GENIChomozygous116378322
7144863039144863040AG17GENIChomozygous115945961
7144864558144864558TTGG7GENIChomozygous128532131
7144864561144864561AG9GENIChomozygous128532132
7144864578144864579T10GENIChomozygous128532133
7144864601144864601G11GENIChomozygous128532134
7144864617144864617A15GENIChomozygous128532135
7144864743144864743T17GENIChomozygous128532136
7144864759144864759G15GENIChomozygous128532137
7144864772144864772T12GENIChomozygous128532138
7144864773144864773GC11GENIChomozygous128532139
7144865001144865001C18GENIChomozygous128532149
7144864770144864771TG12GENIChomozygous118261253
7144857001144857001ATAAATAAATAA18GENIChomozygous134215187
7144864785144864785G7GENIChomozygous128532140
7144864826144864826TC7GENIChomozygous128532141
7144864837144864837T6GENIChomozygous128532142
7144864841144864841T6GENIChomozygous128532143
7144864850144864850A7GENIChomozygous128532144
7144864869144864869C12GENIChomozygous128532145
7144864886144864886A13GENIChomozygous128532146
7144864947144864947T17GENIChomozygous128532147
7144864983144864983T20GENIChomozygous128532148