chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71149111911491120CT26GENIChomozygous115568408
71149159811491599GA43GENIChomozygous115568409
71149172511491726TC31GENIChomozygous115568410
71149180811491809CT32GENIChomozygous115568411
71149199511491996GC26GENIChomozygous115568412
71149232711492328GT45GENIChomozygous115568413
71149284211492843GA31GENIChomozygous115568414
71149287411492875AG35GENIChomozygous115568415
71149335711493358GA16GENICheterozygous115568416
71149336011493361TC15GENICheterozygous115568417
71149357611493577GA33GENIChomozygous115568418
71149379011493791CG6GENICheterozygous115568419
71149392511493926TC29GENIChomozygous115568420
71149406011494061TA28GENIChomozygous115568421
71149412111494122TC27GENIChomozygous115568422
71149448111494482AC40GENIChomozygous115568423
71149488711494888CT47GENIChomozygous115568424
71149546811495469TC27GENIChomozygous115568425
71149561411495615GA20GENIChomozygous115568426
71149563811495639GA29GENIChomozygous115568427
71149575311495754GA28GENIChomozygous115568428
71149596111495962AG27GENIChomozygous115568429
71149597311495974GA28GENIChomozygous115568430
71149599211495993CT31GENIChomozygous115568431
71149636311496364GA32GENIChomozygous115568432
71149636911496370AC30GENIChomozygous115568433
71149661711496618CT17GENIChomozygous115568434
71149685411496855GT25GENIChomozygous115568435
71149699311496994TC32GENIChomozygous115568436
71149708511497086TA47GENIChomozygous115568437
71149732211497323CT24GENIChomozygous115568438
71149746711497468GA33GENIChomozygous115568439
71149748011497481GA29GENIChomozygous115568440
71149787411497875TC40GENIChomozygous115568441
71149790511497906AG46GENIChomozygous115568442
71149812911498130AG34GENIChomozygous115568443
71149816111498162CT42GENIChomozygous115568444
71149847011498471TG34GENIChomozygous115568445
71149873811498739AG30GENIChomozygous115568446
71149891311498914CT21GENIChomozygous115568447