chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115345026115345027TG45GENIChomozygous116666312
8115346133115346133C41GENIChomozygous128634400
8115346931115346932AG41GENIChomozygous116666314
8115347259115347259GGAGGTCAAGGGAGGTCAAG18GENIChomozygous128634401
8115347657115347658AG35GENIChomozygous116666330
8115347694115347695GA38GENIChomozygous116666332
8115347985115347986CT36GENICpossibly homozygous116666334
8115348628115348628CACCCATGACTGACACCCGGCAC37GENIChomozygous128634402
8115348784115348785TC43GENIChomozygous116666344
8115348807115348808TC38GENIChomozygous116666346
8115349094115349095TA49GENIChomozygous116666348
8115350530115350530CTTTTCTTTT33GENIChomozygous128634403
8115351181115351182AG40GENIChomozygous116666350
8115351572115351573G31GENIChomozygous128634404
8115351596115351596T32GENIChomozygous128634405
8115352925115352926CG53GENIChomozygous116666352
8115353766115353766C10GENICheterozygous128634406
8115356380115356381GA56GENIChomozygous116666356
8115357653115357659AGTCCA35GENIChomozygous128634407
8115358094115358095GC25GENICheterozygous132130786
8115358118115358119GA28GENIChomozygous116666358
8115358136115358137TC29GENIChomozygous116666360