chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191147414411474145TC14GENIChomozygous109636727
191147803711478038TC11GENIChomozygous109764845
191147848711478488GA15GENIChomozygous109995441
191148047411480475AG23GENIChomozygous109636731
191148094011480941AG32GENIChomozygous109636733
191148271411482715AC22GENIChomozygous109764847
191148313011483131CA33GENIChomozygous109636735
191148454311484544AG20GENIChomozygous109636737
191148521311485214CG21GENIChomozygous109636739
191148626311486264AG20GENIChomozygous109636741
191148629511486296CT19GENIChomozygous109636743
191149155811491559AT34GENIChomozygous109995448
191149252211492523AG3GENIChomozygous110058400
191149431111494312GA21GENIChomozygous109636755
191149494811494949AG34GENIChomozygous109636759
191149562611495627AT21GENIChomozygous109636761
191149653011496531CT27GENIChomozygous109636763
191149738311497384CT34GENIChomozygous109636765
191149867911498680AC20GENIChomozygous109636769
191149980011499801GT15GENIChomozygous109636771
191150134311501344CT26GENIChomozygous109995452
191150203911502040GC19GENIChomozygous109995454
191150231611502317GA17GENIChomozygous109995457
191150254811502549CA22GENIChomozygous109636775
191150317911503180GT36GENIChomozygous109995459
191150437811504379GT23GENIChomozygous109636777
191150446011504461CT28GENIChomozygous109995461
191150509911505100AG20GENIChomozygous109636781
191150564911505650TC21GENIChomozygous109636785
191150620311506204AG24GENIChomozygous109636795
191150624011506241AG33GENIChomozygous109995463
191150681511506816CT32GENIChomozygous109995465
191149253811492539GA4GENICheterozygous110158249