chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10229995	10229996	A	G	60	GENIC	homozygous	148133062
19	10230033	10230034	T	C	64	GENIC	homozygous	140403421
19	10230256	10230257	G	A	57	GENIC	homozygous	148133063
19	10230597	10230598	T	C	41	GENIC	homozygous	148133064
19	10230656	10230657	C	T	39	GENIC	homozygous	148133065
19	10232343	10232344	C	T	50	GENIC	homozygous	148133066
19	10233348	10233349	G	A	48	GENIC	homozygous	148133067
19	10234081	10234082	T	A	62	GENIC	homozygous	148133068
19	10234159	10234160	G	A	51	GENIC	homozygous	148133069
19	10234920	10234921	C	G	62	GENIC	homozygous	148133070
19	10235095	10235096	T	C	44	GENIC	homozygous	140403460
19	10235616	10235617	T	C	45	GENIC	homozygous	140403465
19	10235624	10235625	T	A	51	GENIC	homozygous	140403466
19	10236077	10236078	T		50	GENIC	homozygous	403442113
19	10236077	10236078	T	G	50	GENIC	heterozygous	403442114
19	10236704	10236705	C	T	42	GENIC	possibly homozygous	147377935
19	10237086	10237087	T	G	51	GENIC	homozygous	140403469
19	10237260	10237261	G	C	24	GENIC	homozygous	140403470