chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148280427182804272TC9GENICpossibly homozygous49017069
148280941482809415GT6GENIChomozygous49017070
148281678582816786CCA1GENIChomozygous49316265
148282329082823291CT8GENICheterozygous49017074
148282883282828833GA8GENICpossibly homozygous49017075
148282942182829422TTAAAA2GENIChomozygous49331995
148283065082830651AG13GENICpossibly homozygous49017078
148283222382832224AAG5GENICheterozygous49017079
148283335482833355GA8GENIChomozygous49017080
148283745782837458AC9GENICpossibly homozygous49017082
148283895782838958TC16GENIChomozygous49017083
148283913282839133TC10GENICheterozygous49017084
148284223682842237C-10GENIChomozygous48811581
148284228782842288C-1GENIChomozygous48811583
148284229982842300TTA4GENIChomozygous48811585
148284236782842368GGA1GENIChomozygous48811587
148284553882845539A-4GENIChomozygous49017086
148284748882847489GA9GENIChomozygous49017087
148284837282848373GA14GENICpossibly homozygous49017088
148284894682848947CCGTGTGTGTGTGT1GENIChomozygous49431032
148285049782850498AG10GENICpossibly homozygous49017089
148285522182855222AG14GENICpossibly homozygous49017090
148285553182855532CA19GENICheterozygous49017091
148285641282856413AG11GENIChomozygous49017092
148286970182869702AG16GENIChomozygous49017093
148287453082874531GGTA2GENICheterozygous48811599
148287482082874821T-4GENIChomozygous48811601
148287681882876821CTT---9GENICheterozygous49017097
148288007582880076A-5GENIChomozygous49017098
148288519782885198CT1GENIChomozygous49017100
148288534882885349T-1GENIChomozygous48811609