chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167450604874506049TA6GENIChomozygous125709797
167450641774506418TG2GENIChomozygous119129395
167450653274506533TA5GENIChomozygous112079200
167453156874531569TC14GENIChomozygous111861103
167452424374524244TA5GENIChomozygous132212800
167453147274531473CG10GENIChomozygous111861101
167453147374531474GC10GENIChomozygous111861102
167453154874531548G10GENIChomozygous129381790
167453149374531493G11GENIChomozygous129381787
167453151074531511T11GENIChomozygous129381788
167453154374531543C10GENIChomozygous129381789
167453160874531609TC18GENIChomozygous111861105
167453161374531614TG19GENIChomozygous111861106
167453161474531615GC19GENIChomozygous111861107
167453808474538085GA1GENIChomozygous125671237
167453808774538087T1GENIChomozygous129381793
167453995674539957CT2GENIChomozygous125671272
167453995874539959CT2GENIChomozygous125671274
167453995974539960TA2GENIChomozygous125671276
167453996874539969TA2GENIChomozygous125671278
167454026174540262CT5GENIChomozygous125671282
167454069974540700GT5GENIChomozygous125709799
167454096774540968CT4GENIChomozygous125709800
167454234574542346TC15GENIChomozygous119129405
167454235974542359A14GENIChomozygous129381794
167454247374542474AG23GENIChomozygous119129407
167454261874542619GA33GENIChomozygous119129409
167454276974542770AG46GENIChomozygous111861110
167454245774542458AT24GENIChomozygous119210762
167454260474542605CT36GENIChomozygous119210763
167454850674548507TC38GENIChomozygous111861124
167454870374548704AG51GENIChomozygous111861126
167455169174551692TC49GENIChomozygous111861137
167455275374552754GT41GENICpossibly homozygous112079202
167455343674553437TG39GENIChomozygous112079204