chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118025684780256848AG19INTERGENIChomozygous50968952
118025754180257542AC15INTERGENIChomozygous50968953
118026662280266623GA35INTERGENIChomozygous50968954
118026921380269214GGATAT24INTERGENIChomozygous50842411
118027265480272655G-16INTERGENICheterozygous50842412
118027282880272829T-7INTERGENIChomozygous50968955
118027285580272856AG8INTERGENIChomozygous50968956
118027322380273224CT28INTERGENIChomozygous50968957
118027340580273406AG27INTERGENIChomozygous50968958
118027360080273601CT31INTERGENICpossibly homozygous50968959
118027360680273607AG28INTERGENIChomozygous50968960
118027427880274279G-12INTERGENIChomozygous50968961
118027477380274774GA18INTERGENIChomozygous50968962
118027485580274856GA20INTERGENIChomozygous50968963
118027515780275158GC29INTERGENIChomozygous50968964
118027556580275566TTA28INTERGENIChomozygous50968965
118027609280276093T-14INTERGENICpossibly homozygous50968966
118027613380276134GA23INTERGENIChomozygous50968967
118027619780276198AG28INTERGENIChomozygous50968968
118027639680276397TC23INTERGENIChomozygous50968969
118027674280276743GA32INTERGENIChomozygous50968970
118027739880277399T-23INTERGENIChomozygous50968971
118027753480277535AG29INTERGENIChomozygous50968972
118027874380278744CT13INTERGENIChomozygous50968973