chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204851419048514191AC40GENIChomozygous109276549
204851446648514467CG29GENICpossibly homozygous109213922
204851519848515199AG34GENIChomozygous109348213
204851532748515328AG28GENIChomozygous109213924
204851546448515465AG3GENIChomozygous119873222
204852180948521810GA17GENIChomozygous119799129
204852184048521841TG15GENICpossibly homozygous119799131
204852196548521966CG21GENIChomozygous109276557
204852196648521967CT21GENIChomozygous109276559
204852213448522135AC24GENIChomozygous109213926
204852224748522248AT10GENIChomozygous109276567
204852233348522334AC18GENIChomozygous109276571
204852234648522347CA7GENIChomozygous109276573
204852274148522742AC26GENIChomozygous109213928
204852286948522870CT27GENIChomozygous109213930
204852299148522992CT23GENIChomozygous109213932
204852307748523078AG27GENIChomozygous109276577
204852316248523163CT14GENIChomozygous109383743
204852337448523375TA27GENIChomozygous109405672
204854964448549645GA21GENIChomozygous119799139
204854993548549936CA15GENIChomozygous119799141
204855001848550019AT13GENIChomozygous119799143
204855022148550222TG20GENIChomozygous119799145
204855022848550229CA19GENIChomozygous119799147
204855093348550934GA20GENIChomozygous109546210
204855106548551066CA15GENIChomozygous119799149