chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6120578691120578692GA30GENIChomozygous54677200
6120579526120579527CCTAT11GENIChomozygous55101091
6120580659120580660TC14GENIChomozygous55101092
6120580812120580813CT17GENIChomozygous55101093
6120580904120580905CT17GENIChomozygous55101094
6120580935120580936GA21GENIChomozygous55101095
6120581051120581052GA15GENIChomozygous55101096
6120581061120581062GA15GENIChomozygous55101097
6120581165120581166GA21GENIChomozygous55101098
6120581217120581225TTTCTTTC--------5GENIChomozygous55908109
6120581604120581605AG22GENIChomozygous55101099
6120581832120581833GA21GENIChomozygous55101100
6120582233120582234AG19GENIChomozygous55101101
6120582634120582635AG15GENICpossibly homozygous55101102
6120582740120582741GA9GENIChomozygous55101103
6120582765120582766TC15GENIChomozygous55101104
6120583116120583117AAT21GENICpossibly homozygous55101105
6120583442120583443CT25GENIChomozygous55101106
6120584763120584764CT25GENIChomozygous55052554
6120585086120585087TC25GENIChomozygous54677210
6120581188120581191TGC---14GENIChomozygous54845124
6120582707120582708GGGTTTTTTTT11GENIChomozygous55429169
6120584022120584023CT10GENIChomozygous55101107
6120584611120584619ACACACAC--------24GENIChomozygous55101108
6120585743120585745CT--23GENIChomozygous55101109