chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159716584497165845AAT5GENICheterozygous722194824
159718118897181189AG8GENICheterozygous588328448
159721500097215001T-11GENIChomozygous722194825
159722540297225403C-4GENIChomozygous722194826
159722541197225412T-6GENIChomozygous722194827
159722577197225772A-19GENICpossibly homozygous722194828
159729052997290530TA1GENIChomozygous588389935
159729053497290535GGA1GENIChomozygous722194829
159729053797290538TTA1GENIChomozygous722194830
159729054297290543AAG1GENIChomozygous722194831
159729271997292720G-3GENIChomozygous722194832
159729477697294777AAT3GENIChomozygous722194833
159730880997308810A-10GENIChomozygous722194836
159730887097308871TTA7GENICheterozygous722194837
159730887897308880AC--6GENICheterozygous722194838
159730888197308882GA2GENIChomozygous588389936
159730888497308885T-2GENIChomozygous722194839
159730888697308887GA1GENIChomozygous588389937
159730889297308893C-1GENIChomozygous722194840
159736199597361996TTC8GENIChomozygous722194841
159736221297362213TTC2GENIChomozygous722194842
159736404297364043GT6GENIChomozygous588328449