chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2246924673246924675GA--22GENIChomozygous59487673
2246925589246925590CT46GENIChomozygous60252519
2246925670246925671C-46GENIChomozygous59487679
2246926128246926129AG39GENIChomozygous59487681
2246926262246926263TC26GENIChomozygous60306624
2246926531246926532TC46GENIChomozygous59487683
2246927747246927748TC38GENIChomozygous59487685
2246928721246928722GA23GENIChomozygous60306625
2246930631246930632GGAA12GENICpossibly homozygous60252520
2246930758246930759GA21GENIChomozygous60252521
2246931141246931142TC32GENIChomozygous59487691
2246931196246931197GA24GENIChomozygous60306626
2246931296246931297TA31GENIChomozygous60252522
2246931430246931496CACACACACACACACACACACACATGTGAGCATACCCACACACACACGCACACATGTGAGCACACC------------------------------------------------------------------11GENICpossibly homozygous60761087
2246932300246932301GC37GENIChomozygous60306627
2246932527246932528CT34GENIChomozygous60252526
2246933023246933024GA33GENIChomozygous59487697
2246934074246934075AACACT21GENIChomozygous59487699
2246934500246934501CA36GENIChomozygous60252527
2246934742246934743A-29GENIChomozygous60306628
2246935620246935621C-16GENIChomozygous60252530
2246935629246935630CA20GENIChomozygous60463242
2246935677246935678CG19GENIChomozygous60463243
2246937074246937075AG35GENIChomozygous60252533
2246938186246938187A-39GENIChomozygous60252534
2246939009246939010AATCC40GENIChomozygous60252537
2246939070246939071TG25GENIChomozygous59487705
2246939461246939463AA--16GENIChomozygous60252538
2246939899246939900AAG15GENICheterozygous60306629
2246939899246939900AAAAG15GENICheterozygous60463244
2246940127246940128AG27GENIChomozygous60252541