chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56078079060780795GCTCG52GENIChomozygous141682657
56078082460780825AG61GENIChomozygous141727800
56078158660781587AT35GENIChomozygous141727801
56078215060782151TA41GENIChomozygous141727802
56078234060782341TG60GENIChomozygous141727803
56078280460782805GA63GENIChomozygous141727804
56078331860783319AG49GENIChomozygous141727805
56078367760783678CT47GENIChomozygous141727806
56078383460783835CT53GENIChomozygous141727807
56078422460784225TG46GENIChomozygous141727808
56078478460784785AG65GENIChomozygous141727809
56078544560785446TC60GENIChomozygous141727810
56078764560787646TA60GENIChomozygous141727811
56078791660787916GGGT21GENIChomozygous141682658
56079205360792054CG63GENIChomozygous137482131
56078313560783135T49GENIChomozygous137311563
56078801460788015CT54GENIChomozygous137482127
56078962560789626TC57GENICpossibly homozygous137482128
56079015960790160AC62GENICpossibly homozygous137482129
56078915160789172TCCTCCTCCTCTTCTTCCTCC23GENIChomozygous143180170
56079212360792124TC61GENIChomozygous137482132
56079255160792552TG69GENIChomozygous137482133
56079290460793005CTGTCATAAGCGTGACAGACTCAAATTAGACCCAGGAAGCCAAGGAAATGCACATTCTAAAGAAGGGGACTGCAAATTAAACTTATAAGACCAATCTTAGA26GENIChomozygous137311564
56079524160795269CAGACACTAGGTATACACAAAGAACATT77GENIChomozygous141682659
56079613560796136CT12GENICpossibly homozygous403143243
56078912360789124CT24GENICheterozygous403143240
56078912360789124C24GENIChomozygous403143241
56079613560796136C12GENICheterozygous403143242
56079322960793230TC67GENIChomozygous137482134
56079345460793455GA59GENIChomozygous137482135
56079616260796163G12GENICheterozygous403143244
56079616260796163GT12GENICpossibly homozygous403143245
56079688960796890AG58GENIChomozygous137482136
56079721460797215AG76GENIChomozygous137482137