chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118025684780256848AG13INTERGENICheterozygous50968952
118027322380273224CT15INTERGENICheterozygous50968957
118027340580273406AG22INTERGENICheterozygous50968958
118027360080273601CT18INTERGENICheterozygous50968959
118027360680273607AG17INTERGENICheterozygous50968960
118027427880274279G-7INTERGENICheterozygous50968961
118027477380274774GA17INTERGENICheterozygous50968962
118027485580274856GA14INTERGENICheterozygous50968963
118027515780275158GC20INTERGENICheterozygous50968964
118027556580275566TTA24INTERGENICheterozygous50968965
118027609280276093T-7INTERGENICheterozygous50968966
118027613380276134GA12INTERGENICheterozygous50968967
118027436880274369TA18INTERGENICheterozygous51170319
118027436480274365T-17INTERGENICheterozygous51021929
118027510380275104CT16INTERGENICheterozygous51021930
118027619780276198AG12INTERGENICheterozygous50968968
118027674280276743GA16INTERGENICheterozygous50968970
118027739880277399T-16INTERGENICheterozygous50968971
118027762180277622CA16INTERGENICheterozygous51293846
118027762280277623AG15INTERGENICheterozygous51293847
118027787680277877CCT13INTERGENICheterozygous51021931
118027804080278041TC21INTERGENICheterozygous51170320
118027804180278042CT21INTERGENICheterozygous51021932
118027874380278744CT14INTERGENIChomozygous50968973