chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118527100118527101CG17GENIChomozygous938647112
8118527665118527666CT24GENIChomozygous938647113
8118527743118527744TC20GENIChomozygous938647114
8118528101118528102CG24GENIChomozygous938647115
8118528190118528191CT22GENIChomozygous938647116
8118528481118528482GA26GENIChomozygous938647117
8118528636118528637TC27GENIChomozygous938647118
8118529030118529031AG28GENIChomozygous938647119
8118529158118529159AG17GENIChomozygous938647120
8118530694118530695TG20GENIChomozygous938647121
8118531195118531196TG9GENIChomozygous938647122
8118531282118531283AG15GENIChomozygous938647123
8118531917118531918GT16GENIChomozygous938647124
8118531931118531932CT16GENIChomozygous938647125
8118532000118532001CT21GENIChomozygous938647126
8118532272118532273CG28GENIChomozygous938647127
8118533158118533159GA30GENIChomozygous938647128
8118534045118534046TC24GENIChomozygous938647129
8118534207118534208TC25GENIChomozygous938647130
8118534265118534266CA18GENIChomozygous938647131
8118534298118534299TC20GENIChomozygous938647132
8118537832118537833CT11GENIChomozygous938647133
8118539275118539276TC19GENIChomozygous938647134
8118539339118539340TC20GENIChomozygous938647135
8118539341118539342CT19GENIChomozygous938647136
8118539596118539597AT28GENIChomozygous938647137
8118540205118540206AT28GENIChomozygous938647138
8118540242118540243GT23GENIChomozygous938647139
8118540281118540282AT27GENIChomozygous938647140