chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	70439296	70439297	G	A	20	GENIC	homozygous	116190345
7	70439914	70439915	C	T	38	GENIC	homozygous	115708976
7	70442832	70442833	C	T	24	GENIC	homozygous	116190354
7	70443589	70443590	C	T	24	GENIC	homozygous	116190356
7	70444787	70444788	A	G	21	GENIC	homozygous	116190358
7	70444803	70444804	T	C	20	GENIC	homozygous	115708978
7	70445651	70445652	C	T	22	GENIC	homozygous	116190366
7	70446222	70446223	G	A	21	GENIC	homozygous	116190368
7	70446910	70446911	A	G	17	GENIC	homozygous	115708979
7	70447868	70447869	T	C	31	GENIC	homozygous	116190370
7	70449738	70449739	A	G	17	GENIC	homozygous	115708982
7	70450425	70450426	A	G	26	GENIC	homozygous	115708983
7	70451014	70451015	C	G	19	GENIC	homozygous	115708984
7	70451570	70451571	A	G	17	GENIC	homozygous	115708985
7	70453142	70453143	T	C	7	GENIC	homozygous	116190372
7	70453484	70453485	G	T	15	GENIC	homozygous	116190374
7	70453696	70453697	T	C	11	GENIC	homozygous	115708986
7	70456380	70456381	C	T	28	GENIC	homozygous	116190376
7	70458992	70458993	C	T	22	GENIC	homozygous	116190384