chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	76360011	76360012	T	C	22	GENIC	homozygous	111095057
17	76360429	76360430	T	C	18	GENIC	homozygous	111419190
17	76360768	76360769	T	A	11	GENIC	homozygous	111419192
17	76363284	76363285	G	T	34	GENIC	homozygous	111095061
17	76363346	76363347	C	T	27	GENIC	homozygous	111095063
17	76365709	76365710	T	C	10	GENIC	homozygous	111095065
17	76365744	76365745	T	C	15	GENIC	homozygous	111095067
17	76365750	76365751	T	C	16	GENIC	homozygous	111095069
17	76367268	76367269	T	C	22	GENIC	homozygous	111095073
17	76370181	76370182	A	G	15	GENIC	homozygous	111095077
17	76370716	76370717	T	G	29	GENIC	homozygous	111095079
17	76371113	76371114	G	A	22	GENIC	homozygous	111095081
17	76373710	76373711	T	C	9	GENIC	homozygous	111095087
17	76373983	76373984	A	C	15	GENIC	homozygous	111095088
17	76375093	76375094	G	A	26	GENIC	homozygous	111095090
17	76376317	76376318	A	G	27	GENIC	homozygous	111095094
17	76376566	76376567	C	T	27	GENIC	homozygous	111095096
17	76377512	76377513	T	C	15	GENIC	homozygous	111095098
17	76377744	76377745	G	T	30	GENIC	homozygous	111095100
17	76380175	76380176	C	T	4	GENIC	homozygous	111419194
17	76380560	76380561	G	T	10	GENIC	homozygous	111095102
17	76381637	76381638	A	G	4	GENIC	homozygous	111095104
17	76381645	76381646	T	C	4	GENIC	homozygous	111095106
17	76382873	76382874	C	G	21	GENIC	homozygous	111095108
17	76383112	76383113	T	C	22	GENIC	homozygous	111095110
17	76383117	76383118	C	T	21	GENIC	homozygous	111095114
17	76383134	76383135	T	C	23	GENIC	homozygous	111095116
17	76383869	76383870	G	A	17	GENIC	homozygous	111095118
17	76384216	76384217	C	T	10	GENIC	homozygous	111095120