chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174518270945182710CT58GENIChomozygous140124663
174518465045184651AT21GENICpossibly homozygous140124665
174518466245184663AT22GENICheterozygous145222122
174518570745185708CT46GENIChomozygous140124666
174518642745186428TA42GENIChomozygous140124667
174518644445186445CT47GENIChomozygous140124668
174518756745187567A38GENICpossibly homozygous140024127
174518980245189802A43GENICpossibly homozygous140024128
174519037845190379GA35GENIChomozygous140124669
174519251145192512GA55GENIChomozygous140124670
174519265745192657CCT36GENIChomozygous140024129
174519268345192684CG36GENIChomozygous140124671
174519305845193059GA49GENIChomozygous140124675
174519286045192861GA21GENIChomozygous140124672
174519291245192913GT28GENIChomozygous140124673
174519292545192926AG31GENIChomozygous140124674
174519336845193369CT41GENIChomozygous140124676
174519342745193427A46GENIChomozygous140024130
174519391545193916CT40GENIChomozygous140124677
174519397045193971AG38GENIChomozygous140124678
174519409945194100AG40GENIChomozygous140124679
174519410245194103TC39GENIChomozygous140124680
174519419445194195GC50GENIChomozygous140124681
174519432445194325GT42GENIChomozygous140124682
174519450045194501AG37GENIChomozygous140124683
174519484645194846CCCCCTC6GENIChomozygous140024131
174519567545195676A2GENICheterozygous145221636
174519577945195786ATGCCCA4GENIChomozygous140024132
174519783045197831TA25GENICpossibly homozygous140124684
174519789245197893CT17GENIChomozygous140124685
174519792245197923CG13GENIChomozygous140124686
174519804145198042AG32GENIChomozygous140124687
174519840745198408CA7GENIChomozygous140124688
174519844645198447TC29GENIChomozygous140124689
174519847345198474GT42GENIChomozygous140124690
174519859145198592CA30GENIChomozygous140124691
174519879345198794GT37GENICpossibly homozygous140124692
174519884445198844G33GENIChomozygous140024133
174519890645198907GA34GENIChomozygous140124693
174519906945199070CT43GENIChomozygous140124694
174519921945199220A48GENIChomozygous140024134