chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154724673154724674TC6GENICheterozygous60900717
1154725203154725204GC10GENICheterozygous60900723
1154725343154725344AG11GENICheterozygous60900724
1154725344154725345TC10GENICheterozygous60900725
1154725406154725407TG10GENICheterozygous60900727
1154725424154725425AC13GENICheterozygous60900729
1154725503154725504GC12GENICheterozygous60900730
1154725517154725518AG12GENICheterozygous60900731
1154725753154725754GC10GENICheterozygous61766725
1154725849154725850CA6GENICheterozygous61766727
1154725975154725976CT11GENICheterozygous60900733
1154726065154726066GT7GENICheterozygous61766729
1154726105154726106TC6GENICheterozygous60900736
1154726320154726321TA11GENICheterozygous61766731
1154726468154726469GA8GENICheterozygous60900739
1154726573154726574CT9GENICpossibly homozygous61766733
1154726735154726848CAGTGGTCAAGACATGGAGTGGGAAAACCCAGGGTGACAGGGAGGGGAGGGTTTGCTCAGTGGTCAAGGCATGGAGTGGGAAACCCCAGGGTGAAAGGGAGGGGAGGGTGGCC-----------------------------------------------------------------------------------------------------------------18GENICheterozygous62444916