chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87892592478925924C8GENIChomozygous138249943
87892622778926228G33GENIChomozygous144813132
87892627478926275AT37GENIChomozygous138350067
87892649778926498CT33GENIChomozygous138350069
87892669978926700AG43GENIChomozygous138350070
87892679978926800GA40GENIChomozygous144824875
87892651378926514CT33GENIChomozygous144824872
87892653778926538CT32GENIChomozygous144824873
87892671478926715GT41GENIChomozygous144824874
87892694878926949GC42GENIChomozygous144824876
87892699878926999AG45GENIChomozygous138350072
87892716278927163CG30GENIChomozygous144824877
87892720278927203AG18GENIChomozygous138350073
87892721978927220GC15GENIChomozygous138350074
87892820478928207AGG46GENIChomozygous144813133
87892906478929065AG27GENIChomozygous138350078
87892771778927718AC46GENIChomozygous144824878
87892774778927748AG41GENIChomozygous144824879
87892796178927962GA29GENIChomozygous144824880
87892940678929407GA48GENIChomozygous138350079
87893021478930215AG53GENIChomozygous144824881
87893138978931390GA36GENIChomozygous144824882
87893211478932115CA45GENIChomozygous144824883
87893369778933698GT28GENIChomozygous144824884
87893394878933949CT37GENIChomozygous144824885
87893561478935615A38GENIChomozygous138249946
87893817378938174AG41GENIChomozygous138350096