chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT18GENIChomozygous638217685
84450321244503213TTA20GENICpossibly homozygous749851127
84450324744503248TC22GENIChomozygous638217686
84450410344504104GC28GENIChomozygous638217687
84450420944504210A-18GENIChomozygous749851128
84450467444504675TC24GENIChomozygous638217688
84450507244505073GGAC27GENIChomozygous749851129
84450510644505107TC41GENIChomozygous638217689
84450530544505306AG20GENIChomozygous638217690
84450532744505328GA20GENIChomozygous638217691
84450568244505683AG34GENIChomozygous638217692
84450660744506608CT31GENIChomozygous638217693
84450710644507107TC35GENIChomozygous638217694
84450710844507109CG35GENIChomozygous638217695
84450777544507776GA26GENIChomozygous638217696
84450792544507926TC18GENIChomozygous638217697
84450808144508082AAT20GENIChomozygous749851130
84450956044509561GA26GENIChomozygous638217698
84450957244509573GT24GENIChomozygous638217699
84450992644509927GC38GENIChomozygous638217700
84451006244510063GA25GENIChomozygous638217701
84451020744510208TC31GENIChomozygous638217702
84451076344510764GA29GENIChomozygous638217703
84451093644510937GGA15GENIChomozygous749851131
84451173744511738AG17GENIChomozygous638217704
84451206744512068AC37GENIChomozygous638217705
84451224844512252ACAC----12GENICheterozygous749851132
84451225044512252AC--12GENICheterozygous749851133
84451292044512921AT11GENIChomozygous638217706
84451299744512998CCTCTT8GENICheterozygous749851136
84451328644513287AC20GENIChomozygous638217707
84451363044513631TA31GENIChomozygous638217708
84451376644513767CCA22GENICpossibly homozygous749851137
84451376644513767CCAA22GENICheterozygous749851138
84451406044514061CT26GENIChomozygous638217709
84451504244515043TC10GENIChomozygous638217710
84451512844515129GA21GENIChomozygous638217711
84451533944515340TTTTTATTTATTTA10GENIChomozygous749851140
84451572844515729CCTGCTTGCTAGGCAAG9GENIChomozygous749851141
84451653744516538AT19GENIChomozygous638217712