chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115141042115141043AG29GENIChomozygous68281305
8115142297115142298CT31GENICheterozygous68884243
8115142327115142328AG42GENICheterozygous68884246
8115142504115142505GA20GENIChomozygous68281307
8115143004115143005GA38GENIChomozygous68281309
8115144171115144172GA41GENIChomozygous68281311
8115144596115144597AG29GENICpossibly homozygous68281313
8115144654115144655GC34GENICheterozygous68281315
8115144674115144675GC34GENICheterozygous68281317
8115144767115144768GA42GENIChomozygous68281319
8115144956115144957AG44GENIChomozygous68281321
8115145004115145005AG27GENIChomozygous68281323
8115145180115145181GA33GENIChomozygous68281325
8115145750115145751TC26GENIChomozygous68281327
8115146418115146419TC31GENICpossibly homozygous68281329
8115146408115146409TC29GENICheterozygous68639309