chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105634097656340977TA14GENIChomozygous52059151
105634163456341635AAG7GENICpossibly homozygous52502530
105634191856341919AAT15GENICpossibly homozygous52059153
105634213756342138T-5GENICheterozygous51891816
105634217956342180TTTG5GENIChomozygous52377761
105634218456342185TTGCTAGGCAAGCGC4GENIChomozygous52377763
105634218856342189G-3GENIChomozygous52377765
105634300556343006G-16GENIChomozygous52059155
105634778456347785GC31GENIChomozygous51654988
105634999756350000TGG---11INTERGENIChomozygous52059157
105635131756351318GGC3GENIChomozygous51460063
105635330756353308AG15GENIChomozygous52059159
105635713856357151AGTGATGCGATCT-------------18GENIChomozygous52059161
105635899356358994CCTGTG2GENIChomozygous52439803
105635914756359149TC--8GENIChomozygous52059163
105636318856363189GA20GENIChomozygous52059165
105636339156363392TC15GENIChomozygous51654994
105636453156364532GA24GENIChomozygous51654996