chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107139488071394881AG46GENICpossibly homozygous116630228
107139499471394995GA43GENICpossibly homozygous117131268
107139532171395322AG20GENICheterozygous118124183
107139532571395326AG20GENICheterozygous118124184
107139675071396751GA40GENIChomozygous117131269
107140150271401503TC57GENIChomozygous116630236
107140298371402984CT57GENIChomozygous116630238
107140374771403748TA36GENIChomozygous117131270
107140860071408601TC42GENIChomozygous116630242
107141078671410787GA42GENIChomozygous117131271
107141373871413739TG43GENIChomozygous116630244
107141441471414415TC45GENIChomozygous117131272
107141742271417423GA53GENICpossibly homozygous117131273
107142156471421565CT38GENIChomozygous117131274
107142206171422062CT57GENIChomozygous117131275
107142373371423734TA50GENIChomozygous116630250
107142721771427218GT40GENICpossibly homozygous116630254
107142812371428124AG43GENIChomozygous116630256
107142857871428579GA43GENIChomozygous117083468
107142859271428593GT42GENIChomozygous116630260
107142869071428691GA40GENIChomozygous116630264
107142872871428729GT27GENIChomozygous117131276
107142875371428754GC31GENIChomozygous117131277
107142894071428941AG35GENIChomozygous118043200
107142894671428947TA35GENICpossibly homozygous118043201
107143024771430248AG29GENIChomozygous117223190
107143129271431293AG40GENIChomozygous116630270
107143312371433124CT38GENIChomozygous116630272
107143326171433262CT54GENIChomozygous116630274
107143498971434990CT55GENICpossibly homozygous117152028
107143516471435165TC57GENICpossibly homozygous116630276
107144040671440407AG47GENIChomozygous116630280
107144109771441098CG28GENIChomozygous117083491
107143024571430246AG27GENIChomozygous117296353
107143005671430057AC29GENIChomozygous116800048