chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	169447957	169447958	T	G	31	GENIC	homozygous	120488036
1	169447960	169447961	G	A	32	GENIC	homozygous	109165351
1	169449654	169449655	T	G	27	GENIC	homozygous	120488037
1	169449655	169449656	A	T	28	GENIC	homozygous	120488038
1	169450967	169450968	T	C	40	GENIC	homozygous	108365519
1	169451011	169451012	T	A	43	GENIC	homozygous	108957456
1	169451312	169451313	T	G	18	GENIC	homozygous	108365521
1	169452052	169452053	A	G	20	GENIC	homozygous	108365523
1	169452612	169452613	C	T	23	GENIC	homozygous	108957457
1	169452615	169452616	A	T	23	GENIC	homozygous	108957458
1	169452991	169452992	C	T	12	GENIC	homozygous	108957459
1	169455697	169455698	C	T	35	GENIC	homozygous	108957460
1	169456335	169456336	T	C	32	GENIC	homozygous	108365528
1	169456694	169456695	G	A	32	GENIC	homozygous	108365530
1	169457674	169457675	T	C	24	GENIC	homozygous	108365532
1	169457762	169457763	C	T	22	GENIC	homozygous	108957461
1	169458159	169458160	A	G	17	GENIC	homozygous	108365534
1	169459677	169459678	C	T	16	GENIC	homozygous	108365536
1	169459705	169459706	C	T	17	GENIC	homozygous	108957462
1	169459907	169459908	G	A	22	GENIC	homozygous	108957463
1	169460661	169460662	G	A	30	GENIC	homozygous	108957464
1	169460957	169460958	C	T	31	GENIC	homozygous	108957465
1	169461647	169461648	A	T	11	GENIC	heterozygous	120523161
1	169461663	169461664	A	C	17	GENIC	homozygous	120488039