chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123595356	123595359	AGG		23	GENIC	homozygous	127925792
3	123595806	123595807	A	G	28	GENIC	homozygous	111692527
3	123596590	123596591	C	T	33	GENIC	homozygous	120084164
3	123596742	123596743	G	A	17	GENIC	homozygous	120084166
3	123597614	123597615	C	T	25	GENIC	homozygous	120084168
3	123597705	123597706	T	C	28	GENIC	homozygous	111692528
3	123597873	123597874	C	T	31	GENIC	homozygous	120084170
3	123598917	123598917		TACTGCGCTCTGGGCCCCGGGG	15	GENIC	homozygous	127925793
3	123598975	123598976	A	C	19	GENIC	homozygous	111692529
3	123600174	123600175	A	G	30	GENIC	homozygous	119987963
3	123601451	123601452	C	T	25	GENIC	homozygous	119987965
3	123601607	123601608	G	A	24	GENIC	homozygous	111692532
3	123601723	123601724	C		14	GENIC	homozygous	131627749
3	123601775	123601776	T	C	13	GENIC	homozygous	119987967
3	123601967	123601968	C	T	23	GENIC	homozygous	119987969
3	123602196	123602196		TTCTGACCT	28	GENIC	homozygous	131627750
3	123602434	123602435	G	C	22	GENIC	homozygous	119987971
3	123602740	123602741	G	C	31	GENIC	homozygous	119987973
3	123603114	123603115	C	T	33	GENIC	homozygous	119987975
3	123603216	123603217	T	C	21	GENIC	homozygous	119987977
3	123603741	123603742	T	C	11	GENIC	homozygous	111692534
3	123604263	123604264	G	A	21	GENIC	homozygous	119987979
3	123604432	123604433	T	C	19	GENIC	homozygous	112447314
3	123606063	123606064	C	G	22	GENIC	homozygous	111692538
3	123606070	123606071	C	T	24	GENIC	homozygous	111692539
3	123606355	123606356	G	A	23	GENIC	homozygous	112447317
3	123607457	123607458	T	C	30	GENIC	homozygous	120084172
3	123606192	123606193	G		30	GENIC	homozygous	134525865