chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104936933849369339GA2GENIChomozygous116882998
104936969949369700CT4GENICheterozygous117410627
104937033849370339GC4GENIChomozygous117129814
104937035049370351GC5GENIChomozygous117059188
104937146249371463CG4GENIChomozygous116883000
104937146949371470AG2GENIChomozygous116883002
104937750749377508TG6GENIChomozygous116883004
104937816049378161CT4GENIChomozygous116883007
104937845849378459AT6GENIChomozygous116883009
104937865049378651AG5GENIChomozygous116883011
104938141249381413TA6GENIChomozygous116883013
104938277049382771CT4GENIChomozygous116883015
104938366449383665CT5GENIChomozygous116883017
104938390249383903AG7GENIChomozygous116883019
104938390649383907AC7GENIChomozygous116883021
104939072349390724TC7GENIChomozygous116883023
104939140649391407GA4GENIChomozygous116883025
104939224349392244GA5GENIChomozygous117009410
104939330549393306GA8GENIChomozygous116883027
104939408749394088AG3GENIChomozygous116883029
104939486949394870TC5GENIChomozygous116883031
104939494749394948GC5GENIChomozygous116883033
104939499349394994AC3GENIChomozygous117195130
104939522049395221TG5GENIChomozygous116883035
104939522149395222TA5GENIChomozygous116883037