chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134851310848513109CT10GENIChomozygous114549313
134851376748513768TA11GENIChomozygous114549314
134851448248514483AC10GENIChomozygous114549315
134851457748514578TC10GENIChomozygous114549316
134852563948525640GC10GENIChomozygous114549317
134852590448525905GA9GENIChomozygous114549318
134852826448528265CT19GENIChomozygous114549319
134852999448529995CA11GENIChomozygous114549320
134853179648531797GA14GENIChomozygous114549321
134853197948531980GA13GENICpossibly homozygous114549322
134853213548532136CT14GENIChomozygous114549323
134853320748533208TG4GENIChomozygous114549324
134853322048533221AG4GENIChomozygous114549325
134853393348533934GA13GENIChomozygous114549326
134853548148535482GA8GENIChomozygous114549327
134853643848536439GA16GENIChomozygous114549328
134853757548537576GA10GENIChomozygous114549329
134853795348537954TC12GENIChomozygous114549330
134853795448537955TC13GENIChomozygous114549331
134853826548538266CG17GENIChomozygous114549332
134853859148538592GC10GENIChomozygous114549333
134853923848539239CT5GENIChomozygous114549334