chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222451893222451894TC16GENIChomozygous108995499
1222452832222452833CT11GENIChomozygous108995500
1222453253222453254CG14GENIChomozygous108995501
1222454261222454262AG14GENIChomozygous108995502
1222454841222454842GC15GENIChomozygous108995503
1222455452222455452AG15GENIChomozygous130833362
1222455489222455490CG10GENIChomozygous108770293
1222455641222455642GA11GENIChomozygous108995506
1222455972222455973AG9GENIChomozygous109449736
1222455975222455976TC3GENIChomozygous130852707
1222455976222455977AG8GENIChomozygous130852708
1222456713222456714CT16GENIChomozygous108995508
1222457760222457761AG10GENIChomozygous108995509
1222458422222458422CAGAGCGGGATC9GENIChomozygous127486149
1222459357222459358T7GENIChomozygous130833363
1222459639222459639C8GENIChomozygous127486150
1222459837222459838CT7GENIChomozygous108546733