chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118093778680937787GC10GENIChomozygous123532733
118094430380944307TGTC2GENIChomozygous128926910
118095638580956386C1GENIChomozygous128926922
118095640480956405C2GENIChomozygous128926923
118095640880956409G2GENIChomozygous128926924
118095643980956439T4GENIChomozygous128926925
118095645980956460A6GENIChomozygous128926926
118095646380956464AT7GENIChomozygous123532754
118095648480956485C10GENIChomozygous128926927
118095649780956497G10GENIChomozygous128926928
118095652180956522T11GENIChomozygous128926929
118095653480956534GG12GENIChomozygous128926930
118095654680956546A13GENIChomozygous128926931
118095659080956590A19GENIChomozygous128926932
118095659780956598CG19GENIChomozygous115918131
118095659880956599GC19GENIChomozygous123532764
118095660180956601A19GENIChomozygous128926933
118095663180956632A20GENIChomozygous128926934
118095663480956635CA20GENIChomozygous116162277
118095663580956636AC20GENIChomozygous116162279
118095667880956678A22GENIChomozygous128926935
118095672080956720G21GENIChomozygous128926936
118095675080956750A17GENIChomozygous128926937
118095675580956755A17GENIChomozygous128926938
118095678180956781A16GENIChomozygous128926939
118095678480956784A16GENIChomozygous128926940
118095684580956846TG14GENIChomozygous118165576
118095687780956877A15GENIChomozygous128926941
118095687980956880AC15GENIChomozygous123532774
118095688080956881CT15GENIChomozygous123532775
118095688380956884TG16GENIChomozygous123532776
118097616280976163GC8GENIChomozygous115996296
118097616480976165GA8GENIChomozygous115996298
118097618480976185GA11GENIChomozygous115996306
118097616780976168GT8GENIChomozygous115996300
118097617380976174GT9GENIChomozygous115996302
118097618280976183GA10GENIChomozygous115996304