chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106383039463830395AG55GENIChomozygous116616556
106383057763830578TA54GENICpossibly homozygous116616558
106383092563830926TC59GENIChomozygous116616560
106383247163832472CT57GENIChomozygous116616562
106383254863832549TC49GENIChomozygous116616564
106383298463832985TC69GENIChomozygous116616566
106383317663833177AT39GENIChomozygous116616568
106383476663834767TC64GENIChomozygous116616570
106383628163836282TA41GENIChomozygous126432267
106383635763836358AG60GENIChomozygous116616572
106383918863839189AG57GENIChomozygous116892106
106384010263840102TAACAGGCCCTGTTTCAAAA63GENIChomozygous128824330
106384150963841510GA43GENIChomozygous116616574
106384157163841572GT50GENIChomozygous116616576
106384157163841571TT50GENIChomozygous128824331
106384330963843310CG35GENIChomozygous116616578
106384364363843643TTTTGTT35GENIChomozygous128824332
106384411663844124TATAGAGA37GENIChomozygous128824333
106384456363844565TT48GENIChomozygous128824334
106384477963844820AATAAATCATAGCCTGATGTTGACATCAGCTGGCCTTGAAC26GENIChomozygous128824335
106384712863847129CT60GENIChomozygous116616580
106384722163847222AG70GENIChomozygous116616582
106384753963847540AT51GENIChomozygous116616584
106384787063847871CT43GENIChomozygous116616586
106384946363849464TC46GENIChomozygous116616588
106385112163851122TC40GENIChomozygous116616590
106385114363851144AG36GENIChomozygous116616592
106385123563851236CT36GENIChomozygous116616594
106385208763852088GA71GENIChomozygous116616596
106385447863854478A34GENIChomozygous128824336
106385487763854878GA43GENIChomozygous116616598
106385542163855422TA41GENIChomozygous117998318
106384011863840119AG53GENIChomozygous117998312
106385052863850529GT51GENICpossibly homozygous117998315
106385450263854503GA44GENIChomozygous117998316
106385457863854579TG62GENIChomozygous117998317
106384334663843346T27GENICheterozygous129969433
106385555863855559GC46GENIChomozygous117998319