chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187146494187146495CT41GENIChomozygous110166966
2187147311187147312AC39GENIChomozygous110166967
2187148150187148151GA37GENIChomozygous110166968
2187148907187148908AG50GENIChomozygous110166969
2187149621187149622AG21GENIChomozygous110166970
2187150174187150175TC36GENIChomozygous110166971
2187150330187150331TC32GENIChomozygous110166972
2187151567187151568GA44GENIChomozygous110166975
2187151799187151800CA40GENIChomozygous110166976
2187152461187152462AG46GENIChomozygous110166977
2187153004187153005TC55GENIChomozygous110166978
2187153114187153115TC45GENIChomozygous110166979
2187153571187153572GC42GENIChomozygous110166980
2187153599187153600GA49GENIChomozygous110166981
2187154184187154185AG54GENIChomozygous110166982
2187154825187154826CT26GENIChomozygous110166984
2187155908187155909GA44GENIChomozygous110166985
2187156064187156065TC42GENIChomozygous110166986
2187154615187154616A25GENICheterozygous132017754
2187150669187150669AAGGAAGG22GENIChomozygous127716663
2187154876187154876CCCTGC34GENIChomozygous127716664