chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118527100118527101CG21GENIChomozygous982763968
8118527665118527666CT24GENIChomozygous982763969
8118527743118527744TC31GENIChomozygous982763970
8118528101118528102CG16GENIChomozygous982763971
8118528190118528191CT17GENIChomozygous982763972
8118528481118528482GA19GENIChomozygous982763973
8118528636118528637TC24GENIChomozygous982763974
8118529030118529031AG32GENIChomozygous982763975
8118529158118529159AG12GENIChomozygous982763976
8118530694118530695TG19GENIChomozygous982763977
8118531282118531283AG29GENIChomozygous982763978
8118532000118532001CT11GENIChomozygous982763979
8118532272118532273CG6GENIChomozygous982763980
8118533158118533159GA21GENIChomozygous982763981
8118534045118534046TC23GENIChomozygous982763982
8118534207118534208TC21GENICpossibly homozygous982763983
8118534265118534266CA25GENIChomozygous982763984
8118534298118534299TC20GENIChomozygous982763985
8118537832118537833CT10GENIChomozygous982763986
8118539275118539276TC25GENIChomozygous982763987
8118539339118539340TC27GENIChomozygous982763988
8118539341118539342CT27GENIChomozygous982763989
8118539596118539597AT16GENIChomozygous982763990
8118540205118540206AT21GENIChomozygous982763991
8118540242118540243GT20GENICpossibly homozygous982763992
8118540281118540282AT17GENIChomozygous982763993