chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71873022	71873022		C	16	GENIC	homozygous	132156517
11	71873698	71873699	C	T	45	GENIC	homozygous	116051434
11	71877254	71877255	G	A	27	GENIC	homozygous	115985382
11	71875064	71875065	G	A	39	GENIC	homozygous	115985378
11	71877796	71877797	A	C	31	GENIC	homozygous	115985384
11	71878581	71878582	C	T	19	GENIC	homozygous	126304352
11	71881327	71881328	C	T	29	GENIC	homozygous	115985388
11	71881503	71881503		A	30	GENIC	possibly homozygous	132156518
11	71882123	71882124	A	G	34	GENIC	homozygous	115985394
11	71882689	71882692	AGA		27	GENIC	homozygous	132156519
11	71882881	71882882	C	T	24	GENIC	homozygous	116051436
11	71884777	71884778	C	T	48	GENIC	homozygous	116051438
11	71885165	71885166	A	C	28	GENIC	homozygous	126319808
11	71885577	71885578	C	T	28	GENIC	homozygous	116051440
11	71886990	71886991	G	A	7	GENIC	homozygous	115985400
11	71887869	71887870	T	C	31	GENIC	homozygous	115985402
11	71887889	71887890	C	G	32	GENIC	homozygous	116051442
11	71887897	71887898	A	G	30	GENIC	homozygous	115985404
11	71888180	71888181	C	T	40	GENIC	homozygous	116051444
11	71888594	71888595	G	C	30	GENIC	homozygous	116051446
11	71888759	71888760	T	C	38	GENIC	homozygous	115985408
11	71889015	71889016	C	T	29	GENIC	homozygous	116051448
11	71889181	71889182	G	C	30	GENIC	homozygous	116051450
11	71885164	71885165	G	A	29	GENIC	homozygous	132163004