chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	36102192	36102193	A	G	14	GENIC	possibly homozygous	51001094
11	36102876	36102877	A	C	18	GENIC	heterozygous	51001095
11	36103026	36103027	C	T	13	GENIC	heterozygous	51001096
11	36103457	36103458	A	G	18	GENIC	homozygous	51001098
11	36103484	36103485	G	A	11	GENIC	possibly homozygous	51001099
11	36103516	36103517	G	A	13	GENIC	heterozygous	51001100
11	36103588	36103589	C	T	7	GENIC	homozygous	51001101
11	36103718	36103719	G	A	10	GENIC	homozygous	51001102
11	36103747	36103748	G	C	7	GENIC	homozygous	51001103
11	36103756	36103757	G	A	7	GENIC	homozygous	51001104
11	36103779	36103780	C	T	14	GENIC	homozygous	51001105
11	36103843	36103844	G	A	16	GENIC	homozygous	51001106
11	36104222	36104223	T	C	2	GENIC	homozygous	51001107
11	36104289	36104290	A	G	11	GENIC	possibly homozygous	51001108
11	36104743	36104744	A	T	20	GENIC	homozygous	51001109
11	36104925	36104926	C	T	8	GENIC	homozygous	51001110
11	36104927	36104928	G	T	9	GENIC	homozygous	51001111
11	36105181	36105182	T	A	8	GENIC	homozygous	51001112
11	36105193	36105194	C	T	7	GENIC	homozygous	51001113
11	36105253	36105254	T	C	11	GENIC	homozygous	50731873
11	36105785	36105786	C	G	19	GENIC	heterozygous	51001114
11	36106211	36106212	A	G	15	GENIC	homozygous	51001115
11	36106381	36106382	C	T	21	GENIC	possibly homozygous	51001116
11	36106407	36106408	C	T	10	GENIC	homozygous	51001117
11	36106412	36106413	T	G	9	GENIC	homozygous	51001118
11	36106492	36106493	A	G	15	GENIC	homozygous	51001119
11	36106525	36106526	G	A	20	GENIC	homozygous	51001120
11	36106570	36106571	T	C	18	GENIC	heterozygous	51001121
11	36106571	36106572	G	A	18	GENIC	heterozygous	51001122
11	36106629	36106630	A	T	12	GENIC	homozygous	51001123
11	36106646	36106647	T	C	10	GENIC	homozygous	51001124
11	36106833	36106834	C	G	21	GENIC	homozygous	51001125
11	36106957	36106958	T	C	6	GENIC	homozygous	51001126
11	36107472	36107473	G	A	5	GENIC	heterozygous	51001127
11	36107475	36107476	G	A	5	GENIC	heterozygous	51001128
11	36107610	36107611	T	G	14	GENIC	possibly homozygous	51001129
11	36107905	36107906	C	G	12	GENIC	possibly homozygous	51001130
11	36108146	36108147	A	G	20	GENIC	possibly homozygous	50731874
11	36108569	36108570	T	C	17	GENIC	homozygous	51001131
11	36108791	36108792	C	T	2	GENIC	homozygous	51001132
11	36108792	36108793	A	T	2	GENIC	homozygous	51001133
11	36108793	36108794	A	G	2	GENIC	homozygous	51001134
11	36108894	36108895	T	A	21	GENIC	possibly homozygous	51001135
11	36109601	36109602	C	CCGG	5	GENIC	heterozygous	51001136
11	36109631	36109632	T	G	20	GENIC	homozygous	51001137
11	36114490	36114491	C	-	6	GENIC	heterozygous	50877802
11	36115958	36115959	C	G	15	GENIC	homozygous	51001139
11	36116340	36116341	C	T	5	GENIC	homozygous	51001140
11	36116499	36116503	TCTT	----	4	GENIC	heterozygous	51001141
11	36116696	36116698	CA	--	2	GENIC	heterozygous	51001143
11	36116697	36116698	A	-	2	GENIC	heterozygous	51179930
11	36116732	36116733	C	G	20	GENIC	possibly homozygous	51001144
11	36116817	36116818	A	-	11	GENIC	homozygous	51001145
11	36116847	36116848	G	A	7	GENIC	homozygous	51001146
11	36116855	36116856	C	T	10	GENIC	possibly homozygous	51001147
11	36116882	36116883	C	G	17	GENIC	possibly homozygous	51001148