chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224144737224144740AAA---19GENIChomozygous57647628
4224146436224146437CT79GENIChomozygous57109425
4224147445224147446TG24GENIChomozygous57109426
4224147654224147655AG57GENIChomozygous57109428
4224147657224147658GC57GENIChomozygous57109430
4224147797224147798TG23GENIChomozygous57109431
4224148371224148372TTG53GENIChomozygous57109433
4224148759224148760AG39GENIChomozygous57109435
4224148764224148765AATATAGGTCTAGAATAGCTCCCC34GENIChomozygous57109436
4224148806224148807GA24GENIChomozygous57109438
4224149153224149154CG64GENIChomozygous57109440
4224149194224149195CT41GENIChomozygous59786793
4224149598224149599TA31GENIChomozygous57109441
4224149735224149736GA31GENIChomozygous57647630
4224150004224150005AAGAAGAG35GENIChomozygous58307010
4224150013224150014GGGAA34GENIChomozygous57109447
4224150565224150566TTA7GENIChomozygous57109449
4224150857224150858AG11GENIChomozygous57109451
4224151280224151281TG30GENIChomozygous57109452
4224152785224152786TA9GENIChomozygous57109465
4224152857224152858TC27GENIChomozygous57109467
4224152975224152976AT28GENIChomozygous57109469
4224153219224153220GA34GENIChomozygous57109470
4224154869224154870TTA9GENICpossibly homozygous57109472
4224155320224155321AAATATAAAT3GENIChomozygous59012975