chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155764163155764164CG28GENIChomozygous114065508
5155764272155764273AG19GENIChomozygous114065510
5155764278155764279AG21GENIChomozygous114065512
5155765981155765982CT27GENIChomozygous114065514
5155766743155766744AT12GENIChomozygous114065518
5155766813155766814CT16GENIChomozygous114065520
5155766853155766854GA12GENIChomozygous114065522
5155767283155767284TC10GENIChomozygous114065524
5155767394155767395TC16GENIChomozygous114065526
5155767883155767884GC21GENIChomozygous114065532
5155768197155768198CA29GENIChomozygous114065534
5155769325155769326AG15GENIChomozygous118846992
5155770622155770623CG15GENIChomozygous114065548