chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95257223752572238TC20GENICpossibly homozygous625661163
95257229152572292GC16GENICpossibly homozygous625661164
95257251652572517CT10GENICpossibly homozygous625661165
95257285452572855GT8GENIChomozygous625661166
95257291752572918GT4GENIChomozygous625661167
95257302652573027CCAGCACGA3GENIChomozygous740873731
95257311552573116CCA3GENIChomozygous740873732
95257419252574193AG14GENIChomozygous625661168
95257448952574490CT11GENICheterozygous625661169
95257469652574697TC17GENIChomozygous625661170
95257473752574738TC14GENICpossibly homozygous625661171
95257489652574897GA19GENICpossibly homozygous625661172
95257512052575121GA18GENICpossibly homozygous625661173
95257545052575451AG19GENIChomozygous625661174
95257567152575672AG3GENIChomozygous625661175
95257628052576281TG8GENIChomozygous625661176
95257632152576322GC10GENICpossibly homozygous625661177
95257661052576611TC11GENIChomozygous625661178
95257665052576651TA19GENIChomozygous625661179
95257683152576832AG21GENICpossibly homozygous625661180
95257701252577013AT19GENIChomozygous625661181
95257741352577414CT10GENIChomozygous625661182
95257750252577503AT17GENICpossibly homozygous625661183
95257762252577623AG9GENIChomozygous625661184
95257765652577657AG8GENIChomozygous625661185
95257847252578473GGA5GENIChomozygous740873733