chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224144737224144740AAA---28GENICpossibly homozygous57647628
4224146436224146437CT18GENIChomozygous57109425
4224147445224147446TG20GENIChomozygous57109426
4224147654224147655AG30GENIChomozygous57109428
4224147657224147658GC30GENIChomozygous57109430
4224147797224147798TG16GENIChomozygous57109431
4224148371224148372TTG21GENIChomozygous57109433
4224148759224148760AG30GENIChomozygous57109435
4224148764224148765AATATAGGTCTAGAATAGCTCCCC28GENIChomozygous57109436
4224148806224148807GA24GENIChomozygous57109438
4224149153224149154CG27GENICpossibly homozygous57109440
4224149598224149599TA32GENIChomozygous57109441
4224149735224149736GA23GENIChomozygous57647630
4224150004224150005AAGAAGAG25GENIChomozygous58307010
4224150013224150014GGGAA26GENIChomozygous57109447
4224150565224150566TTA12GENIChomozygous57109449
4224150857224150858AG24GENIChomozygous57109451
4224151280224151281TG31GENIChomozygous57109452
4224152785224152786TA27GENIChomozygous57109465
4224152857224152858TC15GENIChomozygous57109467
4224152975224152976AT22GENIChomozygous57109469
4224153219224153220GA30GENIChomozygous57109470
4224154869224154870TTA13GENICpossibly homozygous57109472
4224155320224155321AAATATAAAT10GENIChomozygous59012975