chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175703718175703720CA9GENIChomozygous127458370
1175703720175703721AT9GENIChomozygous120474793
1175705164175705165G1GENIChomozygous127458382
1175705173175705173T1GENIChomozygous127458383
1175705175175705177CC2GENIChomozygous127458384
1175705192175705193TG6GENIChomozygous108394803
1175705193175705194CA6GENIChomozygous108394805
1175705202175705202T9GENIChomozygous127458385
1175705204175705204T10GENIChomozygous127458386
1175705208175705209A10GENIChomozygous127458387
1175705218175705219C13GENIChomozygous127458388
1175705237175705238GT23GENIChomozygous108394807
1175705303175705304T33GENIChomozygous127458389
1175705307175705308GA33GENIChomozygous108394809
1175705315175705316GT34GENIChomozygous120474794
1175705316175705317TG34GENIChomozygous120474795
1175705374175705374TC33GENIChomozygous127458390
1175737263175737264C56GENIChomozygous127458396
1175741642175741643G67GENIChomozygous127458402
1175741705175741706G53GENIChomozygous127458403
1175741759175741760C45GENIChomozygous127458404
1175741765175741766A46GENIChomozygous127458405
1175741773175741774A46GENIChomozygous127458406
1175750702175750703C1GENIChomozygous133601036
1175750649175750649A1GENIChomozygous133601031
1175750660175750660C1GENIChomozygous133601032
1175750676175750676A1GENIChomozygous133601033
1175750680175750681C1GENIChomozygous133601034
1175750685175750686C1GENIChomozygous133601035
1175750715175750716C1GENIChomozygous133601037
1175801178175801180TA13GENICheterozygous130214876