chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7107471640107471641C16GENIChomozygous128503576
7107471645107471646C16GENIChomozygous128503577
7107471647107471648CG15GENIChomozygous122836360
7107471649107471649G15GENIChomozygous128503578
7107471651107471652CG16GENIChomozygous118406858
7107471655107471656CG16GENIChomozygous122836362
7107471660107471661TG17GENIChomozygous122836363
7107471667107471668A17GENIChomozygous128503579
7107471669107471670AT16GENIChomozygous118258169
7107471671107471671A16GENIChomozygous128503580
7107471694107471695C13GENIChomozygous128503581
7107471695107471696TG14GENIChomozygous122836367
7107471704107471705AT17GENIChomozygous122836368
7107471707107471707T17GENIChomozygous128503582
7107471719107471719CT17GENIChomozygous128503583
7107471720107471721AC17GENIChomozygous122836371
7107471722107471725ATA17GENIChomozygous128503584
7107471737107471738CT16GENIChomozygous122836373
7107471739107471740CG16GENIChomozygous122836374
7107471741107471742CT16GENIChomozygous122836375
7107471746107471747TG17GENIChomozygous118406859
7107471748107471749TA18GENIChomozygous122836376
7107471749107471750GC18GENIChomozygous122836377
7107471752107471753TG18GENIChomozygous122836378
7107471755107471756TA18GENIChomozygous122836379
7107471759107471760TA19GENIChomozygous118406860
7107471762107471763GT19GENIChomozygous122836380
7107471764107471772GGGGGGAC19GENIChomozygous128503585
7107471775107471776CA17GENIChomozygous118391566
7107471777107471777TTAAATAA17GENIChomozygous128503586
7107471778107471779CA17GENIChomozygous118258171
7107471780107471781CA16GENIChomozygous118258173
7107474126107474126GATTTGAG22GENIChomozygous128503587
7107479915107479915ACT16GENIChomozygous128503589
7107471743107471744CT17GENIChomozygous118405425
7107518566107518567TA5GENIChomozygous115807684
7107527073107527074C6GENIChomozygous128503590
7107518633107518634GA2GENIChomozygous116219256
7107637774107637775A18GENICheterozygous130345537