chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103803483838034839AC26GENIChomozygous116760877
103803670838036709GA47GENIChomozygous116563958
103803674538036746CA50GENIChomozygous116563960
103803692738036928AT43GENIChomozygous116563962
103803692838036929GA43GENIChomozygous116563964
103803703938037040AG35GENIChomozygous116760879
103803726738037268TC24GENIChomozygous117125151
103803755738037558AG47GENIChomozygous117125153
103803939438039395TC45GENIChomozygous117125155
103804017338040174TC37GENIChomozygous116563982
103804022438040225GT49GENIChomozygous116869370
103804064238040643CT35GENIChomozygous116760895
103804086238040863AG24GENIChomozygous116563988
103804089338040894AT26GENIChomozygous116563992
103804195738041958TC28GENIChomozygous116563994
103804208938042090TC28GENIChomozygous116563996
103804218138042182GA48GENIChomozygous116563998
103804289138042892CT37GENIChomozygous116760901
103804312238043123TG31GENIChomozygous116760903
103804375138043752TC43GENIChomozygous116564002
103804403438044035GA19GENIChomozygous116760905
103804419038044191GA34GENIChomozygous116760907
103804444038044441TC27GENIChomozygous116564004
103804544338045444AT23GENIChomozygous116564010
103804553638045537CA27GENIChomozygous116760915
103804558638045587TA36GENIChomozygous116760917
103804590938045910CT32GENIChomozygous116760919
103804630238046303TC27GENIChomozygous116564012
103804666138046662CT19GENIChomozygous117125157
103804669538046696CT18GENIChomozygous116760923
103804931838049319CT20GENIChomozygous116760925
103804940438049405TC33GENIChomozygous116564020
103805071938050720CT32GENIChomozygous117125159
103805117838051179TC29GENIChomozygous116564026
103805261538052616TG10GENIChomozygous116564030
103805321938053220TC26GENIChomozygous116564032