chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	5967439	5967440	C	G	55	GENIC	homozygous	116426130
8	5967707	5967708	C	A	58	GENIC	homozygous	116426131
8	5968348	5968349	C	G	30	GENIC	homozygous	116426134
8	5970836	5970837	C	A	13	GENIC	homozygous	116426135
8	5971028	5971031	TCA		3	GENIC	homozygous	128568630
8	5971037	5971038	G	A	3	GENIC	homozygous	122921866
8	5971039	5971040	C	G	3	GENIC	homozygous	122921867
8	5974598	5974598		CT	55	GENIC	homozygous	128568631
8	5974652	5974653	T	C	40	GENIC	homozygous	116426136
8	5975692	5975704	TGTGTGTGCGTG		12	GENIC	heterozygous	128568632
8	5977211	5977219	GTGAGTGC		24	GENIC	possibly homozygous	128568633
8	5979607	5979608	A	G	48	GENIC	homozygous	116426148
8	5986520	5986521	A	G	50	GENIC	homozygous	116426149
8	5989594	5989595	G	T	44	GENIC	homozygous	116426150
8	5990745	5990766	CACTAAGGGAGATTATTCCTT		39	GENIC	homozygous	128568634
8	5990789	5990790	G	A	43	GENIC	homozygous	116426151
8	5992181	5992182	T	C	63	GENIC	homozygous	116426152
8	5992203	5992204	A	T	60	GENIC	homozygous	116426153
8	5992740	5992741	A	G	51	GENIC	homozygous	116426154