chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141410998214109983TC18GENIChomozygous113659139
141411036414110365GA19GENIChomozygous113659141
141411116214111163AT11GENIChomozygous113575786
141411358114113582CG5GENICheterozygous118794208
141411418314114184GC24GENIChomozygous113659143
141411419314114194TG22GENIChomozygous113659145
141411430214114303AG22GENIChomozygous113351465
141411453914114540CT12GENIChomozygous113659147
141411458414114585GC17GENIChomozygous113659149
141411480814114809AT36GENIChomozygous113659151
141411556114115562CT7GENIChomozygous113659153
141411584814115849CT16GENIChomozygous113659155
141411614414116145AG14GENIChomozygous113659159
141411616114116162GA12GENIChomozygous113659161
141411711314117114GT15GENIChomozygous113659163
141411783614117837AG13GENIChomozygous113659167
141411902914119030GC21GENIChomozygous113659169
141411979114119792AG7GENICheterozygous118829028
141411992114119922TC5GENIChomozygous118780071
141412014714120148CA17GENIChomozygous113659175
141412075014120751CT19GENIChomozygous113351479
141412127514121276AG29GENIChomozygous113351487
141412261114122612GT23GENIChomozygous113659177
141412330414123305AT15GENIChomozygous113659179
141412444414124445AG16GENIChomozygous113659181
141412501514125016CT5GENIChomozygous113659183
141412570014125701CT28GENIChomozygous113659185
141412846914128470GA22GENIChomozygous113659187
141412962614129627GA23GENIChomozygous113659189