chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	93077994	93077995	T	C	82	GENIC	homozygous	50869677
11	93080635	93080636	C	G	36	GENIC	heterozygous	50869678
11	93080637	93080638	G	C	35	GENIC	heterozygous	50869679
11	93080661	93080662	G	C	27	GENIC	heterozygous	50869680
11	93082413	93082414	C	T	37	GENIC	possibly homozygous	50869681
11	93082414	93082415	C	CTT	8	GENIC	heterozygous	50869682
11	93082470	93082471	C	-	39	GENIC	homozygous	50869683
11	93083181	93083182	A	G	63	GENIC	homozygous	50869684
11	93084079	93084080	A	AAT	25	GENIC	homozygous	50869685
11	93084094	93084095	G	GTA	24	GENIC	possibly homozygous	50869686
11	93084349	93084351	AC	--	29	GENIC	heterozygous	50869688
11	93084626	93084627	G	C	50	GENIC	homozygous	50869689
11	93085454	93085456	GT	--	65	GENIC	homozygous	50869690
11	93086351	93086352	A	G	80	GENIC	homozygous	50869691
11	93089463	93089464	C	T	69	GENIC	heterozygous	50899026
11	93089475	93089476	G	A	70	GENIC	heterozygous	50899027
11	93089477	93089478	A	C	69	GENIC	homozygous	50869692
11	93089526	93089527	G	A	95	GENIC	heterozygous	50899028
11	93092070	93092072	CT	--	61	GENIC	homozygous	50869693
11	93092791	93092792	T	C	57	GENIC	homozygous	50869694
11	93101675	93101677	GT	--	12	GENIC	homozygous	50869695
11	93104793	93104794	G	A	48	GENIC	homozygous	50869696
11	93105765	93105766	C	CT	58	GENIC	homozygous	50869697
11	93110510	93110511	T	A	12	GENIC	homozygous	50869698
11	93111275	93111276	A	G	67	GENIC	homozygous	50869699
11	93113194	93113195	C	CACAGTG	32	GENIC	homozygous	50869700
11	93115277	93115278	C	T	49	GENIC	homozygous	50869701