chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215156109215160ACAC----4GENIChomozygous687533387
6109216387109216389GT--20GENIChomozygous687533389
6109216449109216450AC21GENIChomozygous515178690
6109216711109216712CG19GENIChomozygous515178691
6109217708109217709GA16GENIChomozygous515178692
6109217869109217870CCT9GENICheterozygous687533390
6109217869109217870CCTT9GENICheterozygous687533391
6109218078109218079TG23GENIChomozygous515178693
6109218132109218133GA21GENIChomozygous515178694
6109218533109218534TC29GENIChomozygous512055718
6109218971109218972CG30GENIChomozygous515178695
6109219610109219611T-5GENIChomozygous687533392
6109219644109219645CG7GENIChomozygous515178696
6109219668109219669TC7GENIChomozygous515178697
6109219945109219946GA27GENIChomozygous515178698
6109220171109220172AG20GENICpossibly homozygous512055719
6109221203109221204T-4GENIChomozygous687533394
6109221479109221480AG37GENIChomozygous512055720
6109224251109224252CT8GENIChomozygous515178699
6109224345109224346CCTTT11GENICheterozygous687533395
6109224345109224346CCTT11GENICheterozygous687533396
6109224503109224504CT16GENIChomozygous512055721
6109225632109225633TC25GENIChomozygous512055722
6109225969109225970GC27GENIChomozygous512055723
6109226303109226304G-32GENIChomozygous687533397
6109226869109226870T-25GENIChomozygous687533399
6109227067109227069GA--19GENIChomozygous687533400
6109227093109227094CCAG11GENICheterozygous687533401
6109227134109227135GA39GENICheterozygous515178700
6109227138109227139AG39GENICheterozygous515178701
6109227301109227302C-24GENICheterozygous687533402
6109227301109227302CCTGTT21GENIChomozygous687533403
6109227384109227385TC26GENIChomozygous512055724
6109227512109227513TA16GENIChomozygous515178702
6109228010109228011GA24GENIChomozygous515178703