chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4212410502212410503AC11GENICheterozygous565010807
4212413081212413082GA16GENICheterozygous565010808
4212413358212413362CACG----16GENICheterozygous708251705
4212413362212413363TTGC15GENICheterozygous708251706
4212413367212413368GGT12GENICheterozygous708251707
4212413664212413678CTCCCACTCACACA--------------12GENICheterozygous708251709
4212414853212414854T-18GENICheterozygous708251710
4212415451212415452AAT4GENICheterozygous708251711
4212415453212415454GGGTA4GENICheterozygous708251712
4212416050212416051A-17GENICheterozygous708251713
4212416303212416304AAG10GENICheterozygous708251714
4212418567212418568CCTTTG18GENICheterozygous708251716
4212439973212439974GA28GENICheterozygous565010809
4212440850212440851C-6GENICheterozygous708251717
4212468935212468936TG31GENICheterozygous565010810
4212473228212473229TTTTG4GENICheterozygous708251718
4212473649212473651AG--26GENICheterozygous708251719
4212498056212498057TC8GENICheterozygous565010811