chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39181323	39181324	G	A	26	GENIC	homozygous	116799748
8	39182224	39182225	C	G	27	GENIC	homozygous	116799750
8	39183746	39183747	A	T	33	GENIC	homozygous	116799754
8	39184330	39184331	T	G	10	GENIC	homozygous	116799756
8	39184878	39184879	G	A	27	GENIC	homozygous	116799758
8	39185418	39185419	T	C	37	GENIC	homozygous	116462202
8	39185796	39185797	G	A	33	GENIC	homozygous	116799760
8	39186026	39186027	G	T	22	GENIC	homozygous	116462215
8	39187755	39187756	G	A	35	GENIC	homozygous	116799764
8	39188571	39188572	T	C	33	GENIC	homozygous	116462239
8	39189683	39189684	C	A	23	GENIC	homozygous	116799768
8	39189691	39189692	A	T	23	GENIC	homozygous	116799770
8	39190561	39190562	T	G	22	GENIC	homozygous	116462250
8	39192933	39192934	T	G	31	GENIC	homozygous	116799772
8	39193908	39193909	A	G	31	GENIC	homozygous	116462275
8	39196199	39196200	G	A	47	GENIC	homozygous	116799774
8	39197282	39197283	G	A	13	GENIC	homozygous	116799776
8	39198270	39198271	G	A	30	GENIC	homozygous	116799778
8	39201520	39201521	A	C	19	GENIC	homozygous	116462343