chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6100922843100922844CCA24GENIChomozygous54601499
6100923123100923124AATT17GENICpossibly homozygous54601500
6100923123100923124AAT17GENICheterozygous54842710
6100923976100923977TTCG1GENIChomozygous55419733
6100923985100923986GC2GENICheterozygous55651801
6100924058100924059TC9GENIChomozygous54601502
6100924130100924136CAAAAA------7GENICheterozygous54601503
6100924847100924848GA18GENIChomozygous54601505
6100925162100925163AC19GENIChomozygous54601506
6100925323100925324AG25GENIChomozygous54601507
6100925662100925663CT24GENIChomozygous54601508
6100925669100925670TTCC25GENIChomozygous54601509
6100925865100925866AG27GENIChomozygous54601510
6100926587100926588AG14GENIChomozygous54601511
6100926669100926681GTGTGTGTGTGT------------8GENICheterozygous55524095
6100926675100926681GTGTGT------8GENICheterozygous55611436
6100927415100927416T-20GENIChomozygous54601513
6100928659100928660TTAAAC24GENIChomozygous54601514
6100928699100928700GA20GENIChomozygous54601515
6100929828100929829TC21GENIChomozygous54601516
6100930069100930070AG18GENIChomozygous54601517
6100930091100930094CTT---12GENIChomozygous55419739
6100930755100930756AAAT11GENICheterozygous55721686
6100930755100930756AAATAT11GENICheterozygous56581203
6100931098100931099TA23GENIChomozygous54601518