chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148280427182804272TC6GENIChomozygous49017069
148280941482809415GT13GENICheterozygous49017070
148281678882816790AA--2GENICheterozygous49316266
148282118682821187A-4GENICheterozygous49017073
148282329082823291CT21GENICpossibly homozygous49017074
148282883282828833GA15GENICpossibly homozygous49017075
148283065082830651AG23GENICpossibly homozygous49017078
148283222382832224AAG2GENIChomozygous49017079
148283305882833059CCA2GENICheterozygous49470642
148283335482833355GA12GENIChomozygous49017080
148283335582833356TTA4GENICheterozygous49017081
148283745782837458AC9GENIChomozygous49017082
148283895782838958TC21GENIChomozygous49017083
148283913282839133TC13GENIChomozygous49017084
148284223682842237C-9GENICheterozygous48811581
148284228782842288C-7GENIChomozygous48811583
148284229982842300TTA10GENIChomozygous48811585
148284236782842368GGA4GENIChomozygous48811587
148284553882845539A-1GENIChomozygous49017086
148284748882847489GA22GENICpossibly homozygous49017087
148284837282848373GA7GENICpossibly homozygous49017088
148285049782850498AG22GENICpossibly homozygous49017089
148285257082852571A-1GENIChomozygous49347509
148285522182855222AG26GENICpossibly homozygous49017090
148285553182855532CA21GENICpossibly homozygous49017091
148285641282856413AG26GENIChomozygous49017092
148286464082864641A-1GENIChomozygous49331997
148286578082865781A-3GENICheterozygous49347514
148286970182869702AG26GENIChomozygous49017093
148287453082874531GGTA1GENIChomozygous48811599
148287477182874772AAAGAGAG1GENIChomozygous49347523
148287482082874821T-10GENIChomozygous48811601
148287681882876821CTT---11GENICheterozygous49017097
148288007582880076A-7GENIChomozygous49017098
148288519782885198CT9GENIChomozygous49017100