chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104728270147282702GC8GENIChomozygous116878313
104728403047284031TG15GENIChomozygous116587371
104728441047284411CT16GENIChomozygous116587375
104728674747286748AG10GENIChomozygous116878315
104728883547288836AC23GENIChomozygous116773353
104728944447289445CT14GENIChomozygous116773355
104728972247289723AG13GENIChomozygous116773357
104729032647290327AG18GENIChomozygous116587377
104729074347290744GA35GENIChomozygous116773359
104729074547290746CT34GENIChomozygous116773361
104729212247292123CT24GENIChomozygous116773363
104729215347292154TA18GENIChomozygous116878317
104729285447292855CT19GENIChomozygous116773365
104729399347293994GA14GENIChomozygous116878319
104729793047297931CT16GENIChomozygous116773367
104729819447298195GT24GENIChomozygous116773369
104730533547305336TC12GENIChomozygous116773371
104730608547306086AG18GENIChomozygous116773373
104730905447309055GT8GENIChomozygous116773375
104730920547309206AT9GENIChomozygous116587379
104731133847311339TC25GENIChomozygous116773377
104731428847314289AT19GENIChomozygous116878321
104731468547314686GA35GENIChomozygous116773379
104731560947315610TA12GENIChomozygous116773381
104731562947315630GT14GENIChomozygous116773383
104731868947318690TC3GENIChomozygous117078161
104731897947318980CT17GENIChomozygous116878325
104731919047319191GA11GENIChomozygous116773389
104732112447321125AC7GENICheterozygous117078162
104733915847339159GA16GENIChomozygous116878327