chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC49GENIChomozygous503452206
8121845375121845376TC9GENIChomozygous506125845
8121845622121845623TC18GENIChomozygous503452207
8121845798121845799GC30GENIChomozygous503452208
8121847010121847011AG44GENIChomozygous503452209
8121847014121847015CT43GENIChomozygous503452210
8121847292121847293AAC44GENICpossibly homozygous684266289
8121847294121847295AAAAC32GENIChomozygous684266290
8121847356121847357AAAC53GENICpossibly homozygous684266291
8121847499121847500GGAC29GENIChomozygous684266292
8121847589121847590GC12GENICheterozygous506125846
8121848033121848043AAAAAAAAAA----------11GENICheterozygous684266293
8121848289121848290GGA38GENICpossibly homozygous684266294