chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	107174347	107174348	A	G	46	GENIC	homozygous	114936121
6	107178241	107178242	A	C	28	GENIC	homozygous	114936122
6	107178246	107178247	G	C	31	GENIC	homozygous	114936123
6	107187894	107187895	G	T	22	GENIC	homozygous	114936124
6	107190169	107190170	T	C	32	GENIC	homozygous	114936125
6	107190184	107190185	G	T	29	GENIC	homozygous	114936126
6	107190187	107190188	A	C	29	GENIC	homozygous	114936127
6	107190193	107190194	C	A	29	GENIC	homozygous	114936128
6	107193475	107193476	G	T	19	GENIC	homozygous	114936129
6	107194611	107194612	C	A	39	GENIC	possibly homozygous	115076655
6	107195275	107195276	A	T	43	GENIC	heterozygous	115076657
6	107202607	107202608	T	G	9	GENIC	homozygous	114936130
6	107202769	107202770	G	C	5	GENIC	homozygous	115223198
6	107202831	107202832	T	G	15	GENIC	homozygous	114936131
6	107202901	107202902	C	G	11	GENIC	homozygous	114936132
6	107202989	107202990	G	T	27	GENIC	homozygous	114936133
6	107203058	107203059	G	A	22	GENIC	homozygous	114936134
6	107214268	107214269	G	A	24	GENIC	homozygous	114936135
6	107214276	107214277	G	A	26	GENIC	homozygous	114936136
6	107220519	107220520	C	A	31	GENIC	homozygous	114936137
6	107220520	107220521	C	A	31	GENIC	homozygous	115076659
6	107220521	107220522	C	A	33	GENIC	homozygous	115076661
6	107220584	107220585	T	C	34	GENIC	possibly homozygous	114936138
6	107220629	107220630	C	T	39	GENIC	heterozygous	114936139
6	107220655	107220656	C	T	41	GENIC	heterozygous	114936140
6	107220785	107220786	C	T	30	GENIC	heterozygous	115149484