chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145378139145378140GC57GENIChomozygous112870839
4145380213145380214T35GENIChomozygous132967636
4145380277145380278AG20GENIChomozygous112870841
4145380745145380745A37GENIChomozygous132967637
4145380893145380894GA61GENIChomozygous112870842
4145381300145381301AG37GENIChomozygous112870843
4145382075145382076TC40GENIChomozygous112870845
4145382714145382720ACCACT18GENIChomozygous132967638
4145382814145382816CA9GENICheterozygous131363345
4145378927145378928TC44GENIChomozygous119315419
4145379202145379207TTGTC59GENIChomozygous128087975
4145382782145382782CACACT9GENICpossibly homozygous128087979
4145383020145383032CACTCACACACA12GENIChomozygous128087981
4145383063145383063CA22GENIChomozygous128087982
4145384927145384927A28GENIChomozygous128087983
4145386529145386529CAAA31GENIChomozygous128087985
4145386664145386665AG41GENIChomozygous119315421
4145386860145386861AC43GENIChomozygous112870851
4145387719145387720AG51GENIChomozygous112870852
4145388065145388066GC29GENIChomozygous119315422
4145389001145389002GA53GENIChomozygous119315423
4145389739145389740TC51GENIChomozygous119412368