chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118527100118527101CG20GENIChomozygous941556061
8118527665118527666CT26GENIChomozygous941556062
8118527743118527744TC16GENIChomozygous941556063
8118528101118528102CG21GENIChomozygous941556064
8118528190118528191CT29GENIChomozygous941556065
8118528481118528482GA23GENIChomozygous941556066
8118528636118528637TC32GENIChomozygous941556067
8118529030118529031AG22GENIChomozygous941556068
8118529158118529159AG32GENIChomozygous941556069
8118530694118530695TG24GENIChomozygous941556070
8118531282118531283AG28GENIChomozygous941556071
8118531885118531886AG20GENIChomozygous941556072
8118531917118531918GT21GENIChomozygous941556073
8118532000118532001CT14GENIChomozygous941556074
8118532272118532273CG17GENIChomozygous941556075
8118533158118533159GA34GENIChomozygous941556076
8118534045118534046TC46GENIChomozygous941556077
8118534207118534208TC32GENIChomozygous941556078
8118534265118534266CA27GENIChomozygous941556079
8118534298118534299TC28GENIChomozygous941556080
8118537832118537833CT28GENIChomozygous941556081
8118539339118539340TC29GENIChomozygous941556082
8118539596118539597AT19GENIChomozygous941556083
8118540205118540206AT20GENIChomozygous941556084
8118540242118540243GT19GENIChomozygous941556085
8118540281118540282AT28GENIChomozygous941556086