chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105457162754571628A54GENICpossibly homozygous142203467
105457178754571788AG59GENIChomozygous142248119
105457190254571903AG70GENIChomozygous142248120
105457190854571909AG69GENIChomozygous142248121
105457227754572278AG58GENIChomozygous142248122
105457235354572354AG60GENIChomozygous142248123
105457394554573946GA46GENIChomozygous142248124
105457481054574811GT48GENIChomozygous142248125
105457486354574864TG40GENIChomozygous142248126
105457569954575701TA46GENIChomozygous142203468
105457595554575956GA40GENIChomozygous142248127
105457602654576027GA56GENIChomozygous142248128
105457624254576243AG45GENIChomozygous142248129
105457668754576688AG42GENIChomozygous142248130
105457670554576706TC40GENIChomozygous142248131
105457706754577068TC53GENIChomozygous142248132
105457759454577594GAAG36GENIChomozygous142203469
105457778054577781AG54GENIChomozygous142248133
105457909954579100GC26GENIChomozygous403286954
105457909754579098G26GENICheterozygous403286951
105457909754579098GC26GENIChomozygous403286952
105457909954579100G26GENICheterozygous403286953
105457910154579102GC26GENIChomozygous142248134
105457910354579104GC16GENICheterozygous145741341
105457910554579106GC18GENICheterozygous146229843
105457924854579249GA45GENIChomozygous142248135
105457943454579435CT45GENIChomozygous142248136
105457951854579519GA38GENIChomozygous142248137
105458040354580404GA68GENIChomozygous142248138