chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139629703139629704CCCACCATGCCCAGTCTGGAGACATTCATTTGTCTTCCTTTCTCAGGGTTCTCTAGAGTCACATATCTTATGGAATGACTATCTATCTATCTATCTATCTATCTATCTATCTATCTAT27GENICpossibly homozygous56355002
5139629730139629731GC34GENICheterozygous55750065
5139630237139630239AA--4GENICheterozygous56493785
5139638008139638009GGT1GENIChomozygous56532193
5139656029139656030G-17GENIChomozygous56457482
5139656032139656033GGT17GENIChomozygous56457483
5139656042139656043G-16GENIChomozygous55750118
5139656055139656056G-14GENIChomozygous55750119
5139656089139656090CT19GENIChomozygous55750120
5139656095139656096GT22GENIChomozygous55750121
5139656099139656100TG20GENIChomozygous55750122
5139656129139656130A-27GENIChomozygous55750123
5139656153139656154AC34GENIChomozygous55750124
5139656167139656168CT31GENIChomozygous55750125
5139656172139656173AT33GENIChomozygous55750126
5139658647139658648TTA9GENICheterozygous55904833
5139660268139660269CCT27GENIChomozygous55750131
5139660271139660272AAC26GENIChomozygous55750132
5139660281139660282CCA28GENIChomozygous55750133
5139660288139660289AAAC25GENIChomozygous55750134
5139660323139660324CCA32GENIChomozygous55750135
5139661034139661035GGT26GENIChomozygous55750139