chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115255608115255609AC22GENIChomozygous112815031
4115258594115258595TC23GENIChomozygous112815035
4115258679115258680GC32GENIChomozygous112815037
4115258687115258688GA29GENIChomozygous112815039
4115261930115261931AG19GENIChomozygous112815043
4115262141115262142GA17GENIChomozygous112815045
4115265585115265586AG36GENIChomozygous112815047
4115269353115269354CT34GENIChomozygous112815049
4115270254115270255GA29GENIChomozygous112815051
4115270764115270765AC23GENIChomozygous112815053
4115271633115271634AC36GENIChomozygous112815055
4115272999115273000AC32GENIChomozygous112815059
4115274349115274350CG26GENIChomozygous112815061
4115274808115274809TC34GENIChomozygous112815063
4115275324115275325GT33GENIChomozygous112815065
4115275502115275503GT29GENIChomozygous112815067
4115275511115275512GA32GENIChomozygous112815069
4115275873115275874GA17GENIChomozygous112815071
4115276334115276335TC31GENIChomozygous112815073
4115276963115276964CT28GENIChomozygous112815075
4115276986115276987GA26GENICpossibly homozygous119454567
4115277336115277337GC37GENIChomozygous112815077