chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
203250356832503569A-39GENICheterozygous691665053
203250597432505975TTGC23GENIChomozygous691665054
203250754332507544CCA28GENIChomozygous691665056
203250868232508683C-27GENIChomozygous691665057
203250874932508750C-40GENIChomozygous691665058
203251236332512364AC7GENIChomozygous522336219
203251302832513029CCT11GENICpossibly homozygous691665059
203253177432531775A-16GENIChomozygous691665060
203253177732531778TTAA12GENIChomozygous691665061
203253183932531840CT8GENIChomozygous521467993
203253185932531860C-3GENIChomozygous691665062
203253187032531871CCA2GENIChomozygous691665063
203253189332531894CA4GENIChomozygous521467994
203253189732531898CA4GENIChomozygous522336220
203253190032531901CCT4GENIChomozygous691665064
203253191232531913AAC4GENIChomozygous691665065
203253191632531917AC5GENIChomozygous522336221
203253191932531920CA5GENIChomozygous521467995
203253193032531931GGC4GENIChomozygous691665066
203253195432531955CA9GENICpossibly homozygous522336222
203253195832531959G-6GENIChomozygous691665067
203253521032535211AAAC7GENICpossibly homozygous691665068