chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160328202160328203GA16GENIChomozygous114074083
5160329735160329736CT30GENIChomozygous114074084
5160332931160332932CG24GENIChomozygous114074085
5160333141160333142TC26GENIChomozygous114074086
5160333684160333685CG18GENIChomozygous114074087
5160334201160334202AC35GENIChomozygous114074088
5160335239160335240AT16GENIChomozygous114074089
5160335433160335434GC24GENIChomozygous114074090
5160336588160336589GA15GENIChomozygous114074091
5160337021160337022GA21GENIChomozygous114074092
5160337537160337538CA18GENIChomozygous114074093
5160338349160338350TA25GENIChomozygous114074095
5160342087160342088AG23GENIChomozygous114074097
5160342408160342409AG27GENIChomozygous114074098
5160342576160342577CA26GENIChomozygous114074099
5160342711160342712CT16GENIChomozygous114074100
5160344291160344292GA18GENIChomozygous114074101
5160345160160345161AC29GENIChomozygous114074102
5160345424160345425CT20GENIChomozygous114074103
5160345676160345677AG18GENIChomozygous114074104
5160345806160345807AG15GENIChomozygous114074105
5160346657160346658AG24GENIChomozygous114074106
5160346739160346740TC26GENIChomozygous114074107
5160350090160350091AG13GENIChomozygous114074108
5160350280160350281GA19GENIChomozygous114074109