chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124149915124149916CT21GENIChomozygous118360429
7124149957124149958CT30GENIChomozygous118360431
7124150037124150038CT29GENIChomozygous118360433
7124150591124150592GA10GENIChomozygous118360435
7124151246124151247CT24GENIChomozygous118360437
7124151451124151452CA43GENIChomozygous118360439
7124153135124153136CT20GENIChomozygous118360441
7124153348124153349TC23GENIChomozygous118360443
7124153400124153401AT17GENIChomozygous118360445
7124153556124153557AG15GENIChomozygous118360447
7124153834124153835AG20GENIChomozygous118360449
7124154303124154304AG16GENIChomozygous118360451
7124154642124154643CA29GENIChomozygous118360453
7124156269124156270CT17GENIChomozygous118360455
7124157928124157929TC27GENIChomozygous118360457
7124158761124158762TC26GENIChomozygous115865087
7124161547124161548TC31GENIChomozygous118360459
7124162164124162165CT17GENIChomozygous118525361
7124163970124163971CG24GENIChomozygous115865099
7124164234124164235GC16GENIChomozygous115865103
7124164390124164391CT20GENIChomozygous116082824
7124164391124164392TA19GENIChomozygous118322471
7124165208124165209GC41GENIChomozygous115865113
7124172669124172670GT29GENIChomozygous116410070
7124174752124174753CA25GENIChomozygous115865133
7124175205124175206TC23GENIChomozygous115865135
7124176554124176555TC22GENIChomozygous115865137
7124176576124176577CT28GENIChomozygous116410072
7124176612124176613AG25GENIChomozygous115865139
7124188366124188367CT18GENIChomozygous116410075
7124189380124189381GA35GENIChomozygous116410076
7124190488124190489TC21GENIChomozygous115865157
7124190774124190775TC28GENIChomozygous115865159
7124191153124191154CT21GENIChomozygous115865161
7124193004124193005CA15GENICpossibly homozygous115865165
7124193458124193459AG30GENIChomozygous118360462
7124193629124193630AG26GENIChomozygous115865167
7124193782124193783CT25GENIChomozygous118360464
7124194600124194601AG5GENIChomozygous115865177