chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6126434653126434654TC11GENIChomozygous118734360
6126435353126435354AG13GENIChomozygous118734361
6126435436126435437AT18GENIChomozygous118734362
6126436303126436304TC17GENIChomozygous118734363
6126436397126436398TG8GENIChomozygous118734364
6126436410126436411GA5GENIChomozygous118734365
6126436867126436868CT21GENIChomozygous118734366
6126436942126436943CT15GENIChomozygous118734367
6126436979126436980GT12GENIChomozygous118734368
6126437097126437098GC10GENIChomozygous118734369
6126437098126437099GA9GENIChomozygous118734370
6126437142126437143GC10GENIChomozygous118734371
6126437273126437274GT9GENIChomozygous118734372
6126437408126437409CT11GENIChomozygous118734373
6126438103126438104CT15GENIChomozygous118734374
6126438201126438202TC18GENIChomozygous118734375
6126438724126438725TC19GENIChomozygous118734376
6126438779126438780GA24GENIChomozygous118734377
6126440821126440822CT18GENIChomozygous118734378
6126442622126442623AG18GENIChomozygous118734379
6126443655126443656GA10GENIChomozygous118734380
6126443680126443681AG11GENIChomozygous118734381
6126443757126443758CT9GENIChomozygous118734382
6126445114126445115GA9GENIChomozygous118734383
6126445409126445410GT15GENIChomozygous118734384