chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31651684	31651685	T	G	35	GENIC	homozygous	116547184
10	31652538	31652539	T	G	11	GENIC	homozygous	116547190
10	31653256	31653256		T	33	GENIC	possibly homozygous	133227043
10	31653509	31653510	T	C	53	GENIC	homozygous	116547192
10	31654788	31654789	T	A	43	GENIC	homozygous	116547194
10	31656223	31656224	A		33	GENIC	homozygous	128803703
10	31656237	31656238	T		34	GENIC	homozygous	128803704
10	31656475	31656475		CCC	40	GENIC	homozygous	128803705
10	31657153	31657154	T	A	45	GENIC	homozygous	116547196
10	31658263	31658264	C	G	12	GENIC	homozygous	117002194
10	31658407	31658409	AT		11	GENIC	homozygous	128803707
10	31658413	31658414	T	A	11	GENIC	homozygous	123436103
10	31658422	31658422		C	12	GENIC	homozygous	128803708
10	31658435	31658435		A	14	GENIC	homozygous	128803709
10	31658445	31658445		T	18	GENIC	homozygous	128803710
10	31658754	31658755	G	T	38	GENIC	homozygous	117002196
10	31658755	31658756	A	T	37	GENIC	homozygous	117002198
10	31658831	31658832	G		38	GENIC	homozygous	128803711
10	31659038	31659039	T	A	39	GENIC	homozygous	116547204
10	31659433	31659434	T	G	44	GENIC	homozygous	116547208
10	31659766	31659766		AC	48	GENIC	homozygous	133227044