chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141503097141503098G-31GENIChomozygous54159157
7141503728141503729GT56GENIChomozygous54266808
7141504099141504100AT33GENIChomozygous54159158
7141504453141504454G-28GENIChomozygous54159159
7141504454141504456GC--28GENIChomozygous54159160
7141504628141504629GA40GENIChomozygous54266811
7141504994141504995CG35GENIChomozygous54266814
7141505443141505444GA48GENIChomozygous54266818
7141505470141505471GA51GENIChomozygous54266821
7141505545141505546AC31GENIChomozygous54266824
7141506142141506143TTG1GENIChomozygous54266827
7141506337141506338T-26GENIChomozygous54266830
7141507035141507036AG37GENIChomozygous54159163
7141507235141507236CT24GENIChomozygous54266833
7141508107141508108CA23GENIChomozygous54266836
7141508306141508307TTACACAC11GENIChomozygous54159167
7141508755141508756GA39GENIChomozygous54266839
7141509514141509515AG20GENIChomozygous54159169
7141509890141509891A-47GENIChomozygous54266852
7141510823141510824C-34GENIChomozygous54159171
7141512990141512991GA44GENIChomozygous54266855
7141513148141513149CCTA40GENIChomozygous54159172
7141513308141513309TC30GENIChomozygous54159173
7141513363141513364GA31GENIChomozygous54266858
7141513695141513696AG33GENIChomozygous54266861
7141514011141514012GA38GENIChomozygous54266864
7141514234141514235CT43GENIChomozygous54266867
7141515197141515198GA44GENIChomozygous54266870
7141515309141515310GC45GENIChomozygous54159175
7141515698141515699AG43GENIChomozygous54159176
7141515839141515840GC23GENIChomozygous54159177
7141516086141516087CCAT4GENICheterozygous54159178
7141516091141516092G-8GENICheterozygous54159179
7141516091141516092GGT6GENICheterozygous54159180
7141516091141516092GGGT6GENICheterozygous54159181
7141516158141516159GA24GENICpossibly homozygous54266873
7141516261141516262GA32GENICpossibly homozygous54266876
7141516572141516573GA36GENIChomozygous54266879
7141516844141516845CG47GENIChomozygous54266883