chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148773896148773897A17GENICheterozygous127941162
3148774189148774190CA15GENIChomozygous111770855
3148774266148774266GCGGGTCCTT15GENIChomozygous127941163
3148787175148787176AG30GENICheterozygous111770920
3148787176148787177CT31GENICheterozygous111770922
3148787190148787191CG31GENICheterozygous111770924
3148787668148787668CT17GENIChomozygous127941172
3148787698148787699G14GENIChomozygous127941173
3148787700148787701T14GENIChomozygous127941174
3148787735148787735G14GENIChomozygous127941175
3148787748148787748C11GENIChomozygous127941176
3148787769148787769A10GENIChomozygous127941177
3148787778148787779TG8GENIChomozygous120065709
3148787779148787780AT8GENIChomozygous120065711
3148787810148787810C5GENIChomozygous127941178
3148787812148787813TG5GENIChomozygous119714970
3148787816148787816A3GENIChomozygous127941179
3148787823148787824TA3GENIChomozygous119841751
3148787824148787825AT3GENIChomozygous119721508
3148787827148787828TG3GENIChomozygous119841752
3148787832148787833G3GENIChomozygous127941180
3148790054148790054ACTAGACATGGTGGCACATGCCTGGGATGCTGCC27GENIChomozygous127941182
3148790193148790193G28GENIChomozygous127941183
3148790202148790202G31GENIChomozygous127941184
3148791011148791011CCCCAA10GENIChomozygous127941185
3148797868148797868ACATTACATG27GENIChomozygous127941188
3148787848148787849G3GENIChomozygous129892203