chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	101288604	101288605	T	G	43	GENIC	possibly homozygous	116983364
10	101289526	101289527	G		9	GENIC	homozygous	128853913
10	101290387	101290388	G		17	GENIC	homozygous	128853916
10	101290392	101290392		C	15	GENIC	homozygous	128853917
10	101291337	101291338	G	T	34	GENIC	possibly homozygous	116983366
10	101289557	101289557		CG	8	GENIC	homozygous	132694547
10	101289562	101289562		CC	8	GENIC	homozygous	132694548
10	101289563	101289563		A	7	GENIC	homozygous	132694549
10	101292625	101292637	AGAAAGAGAGAA		19	GENIC	homozygous	132694550
10	101293093	101293094	T		29	GENIC	homozygous	132694551
10	101289565	101289566	T	A	7	GENIC	homozygous	116709437
10	101289574	101289575	A	T	6	GENIC	homozygous	116709439
10	101292743	101292743		AT	36	GENIC	possibly homozygous	131097671
10	101293612	101293613	T	C	36	GENIC	homozygous	116957901