chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148280427182804272TC13GENIChomozygous49017069
148280941482809415GT20GENIChomozygous49017070
148281022082810221TTA2GENICheterozygous49421281
148282329082823291CT13GENICpossibly homozygous49017074
148282883282828833GA18GENICpossibly homozygous49017075
148283065082830651AG14GENIChomozygous49017078
148283335482833355GA2GENIChomozygous49017080
148283335582833356TTA3GENICheterozygous49017081
148283745782837458AC5GENIChomozygous49017082
148283895782838958TC21GENIChomozygous49017083
148283913282839133TC23GENICpossibly homozygous49017084
148284223682842237C-10GENIChomozygous48811581
148284228782842288C-10GENIChomozygous48811583
148284229982842300TTA13GENIChomozygous48811585
148284236782842368GGA3GENIChomozygous48811587
148284553882845539A-1GENIChomozygous49017086
148284748882847489GA1GENIChomozygous49017087
148284837282848373GA5GENIChomozygous49017088
148285049782850498AG17GENIChomozygous49017089
148285522182855222AG29GENIChomozygous49017090
148285553182855532CA11GENICpossibly homozygous49017091
148285641282856413AG22GENIChomozygous49017092
148286578082865781A-2GENICheterozygous49347514
148286970182869702AG17GENICpossibly homozygous49017093
148287482082874821T-3GENICheterozygous48811601
148287681882876821CTT---14GENICpossibly homozygous49017097
148288007582880076A-5GENIChomozygous49017098
148288519782885198CT3GENIChomozygous49017100