chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109145253491452535AC15GENIChomozygous961780109
109145325291453253GT29GENIChomozygous961780110
109145401791454018AG28GENIChomozygous961780111
109145504291455043CG23GENIChomozygous961780112
109145569791455698GA34GENIChomozygous961780113
109145739991457400GA28GENIChomozygous961780114
109146089391460894CT33GENIChomozygous961780115
109146235091462351AT23GENIChomozygous961780116
109146307491463075GA49GENIChomozygous961780117
109146347391463474AG38GENIChomozygous961780118
109146372391463724TC24GENIChomozygous961780119
109146372691463727CT25GENIChomozygous961780120
109146524091465241AT27GENIChomozygous961780121
109146694991466950AC40GENIChomozygous961780122
109146712991467130TC26GENIChomozygous961780123
109146851291468513AG24GENIChomozygous961780124
109146889991468900AG32GENIChomozygous961780125
109147180091471801CT31GENIChomozygous961780126
109147335491473355TG38GENIChomozygous961780127
109147437191474372CA45GENIChomozygous961780128
109147596891475969AT20GENIChomozygous961780129
109148174591481746CG35GENIChomozygous961780130
109148179391481794GA38GENIChomozygous961780131
109148230891482309TC22GENIChomozygous961780132
109148311991483120TC20GENIChomozygous961780133
109148319691483197TC15GENIChomozygous961780134
109148336891483369TG22GENIChomozygous961780135
109148898891488989TC18GENIChomozygous961780136
109149039291490393GA23GENIChomozygous961780137
109149048491490485CG37GENIChomozygous961780138
109149080191490802GA8GENIChomozygous961780139
109149163791491638CT16GENIChomozygous961780140
109149416091494161CT30GENIChomozygous961780141
109149442091494421CT24GENIChomozygous961780142
109149447991494480GA23GENICpossibly homozygous961780143
109149561791495618TC17GENIChomozygous961780144
109149564991495650GT22GENIChomozygous961780145
109149737791497378AT19GENIChomozygous961780146
109149809391498094TC23GENIChomozygous961780147