chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	101288613	101288614	T	-	19	GENIC	homozygous	52936568
10	101288969	101288971	TA	--	1	GENIC	homozygous	53173225
10	101289024	101289025	G	A	18	GENIC	homozygous	53173226
10	101289221	101289222	A	G	26	GENIC	homozygous	52936570
10	101289613	101289614	G	A	12	GENIC	homozygous	52936572
10	101290316	101290317	A	G	25	GENIC	homozygous	52936576
10	101290422	101290423	T	TC	19	GENIC	homozygous	52936578
10	101290645	101290646	A	G	21	GENIC	homozygous	52936581
10	101290728	101290729	T	C	36	GENIC	homozygous	52936583
10	101290867	101290868	G	T	30	GENIC	homozygous	52936585
10	101291112	101291113	G	A	36	GENIC	homozygous	52936587
10	101291117	101291118	G	A	33	GENIC	homozygous	52936589
10	101291183	101291184	G	A	31	GENIC	homozygous	52936591
10	101291294	101291295	T	C	23	GENIC	homozygous	52936593
10	101291297	101291298	A	G	25	GENIC	homozygous	52936595
10	101291413	101291414	G	C	11	GENIC	homozygous	53173227
10	101291419	101291420	A	G	13	GENIC	homozygous	51581700
10	101291630	101291631	T	A	30	GENIC	homozygous	53173228
10	101291748	101291749	C	T	27	GENIC	homozygous	51581704
10	101291852	101291853	T	C	16	GENIC	homozygous	51581706
10	101291878	101291879	C	G	19	GENIC	homozygous	51581708
10	101292217	101292218	C	T	30	GENIC	homozygous	52936597
10	101292427	101292428	G	A	18	GENIC	possibly homozygous	53173229
10	101293047	101293048	T	C	32	GENIC	homozygous	51581710
10	101293667	101293668	C	CGTGT	6	GENIC	homozygous	52969049