chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167450583274505835CTT5GENIChomozygous132207757
167450604874506049TA4GENIChomozygous125709797
167450641774506418TG9GENIChomozygous119129395
167450653274506533TA26GENIChomozygous112079200
167452402774524030CTT4GENIChomozygous132207758
167452424374524244TA9GENIChomozygous132212800
167453147274531473CG21GENIChomozygous111861101
167453147374531474GC21GENIChomozygous111861102
167453154874531548G22GENIChomozygous129381790
167453149374531493G26GENIChomozygous129381787
167453151074531511T26GENIChomozygous129381788
167453154374531543C21GENIChomozygous129381789
167453156874531569TC25GENIChomozygous111861103
167453160874531609TC25GENIChomozygous111861105
167453161374531614TG25GENIChomozygous111861106
167453161474531615GC25GENIChomozygous111861107
167453790474537905TA4GENIChomozygous125709798
167454026174540262CT9GENIChomozygous125671282
167454069974540700GT4GENIChomozygous125709799
167454096774540968CT2GENIChomozygous125709800
167454234574542346TC17GENIChomozygous119129405
167454235974542359A17GENIChomozygous129381794
167454245774542458AT17GENIChomozygous119210762
167454247374542474AG17GENIChomozygous119129407
167454260474542605CT64GENIChomozygous119210763
167454261874542619GA73GENIChomozygous119129409
167454276974542770AG28GENIChomozygous111861110
167454850674548507TC44GENIChomozygous111861124
167454870374548704AG42GENIChomozygous111861126
167455169174551692TC50GENIChomozygous111861137
167455275374552754GT41GENICpossibly homozygous112079202
167455343674553437TG59GENIChomozygous112079204