chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	132374007	132374008	C	G	8	GENIC	homozygous	115081047
6	132374010	132374011	G	A	5	GENIC	homozygous	115081048
6	132374026	132374027	T	A	3	GENIC	homozygous	115081049
6	132374328	132374329	T	C	40	GENIC	homozygous	114990359
6	132374329	132374330	T	C	41	GENIC	homozygous	114990361
6	132374412	132374413	T	G	54	GENIC	homozygous	114990363
6	132384019	132384020	C	G	43	GENIC	heterozygous	115507570
6	132387394	132387395	T	G	33	GENIC	heterozygous	115166233
6	132420197	132420198	C	A	20	GENIC	possibly homozygous	114990367
6	132424389	132424390	T	A	41	GENIC	homozygous	114990369
6	132430783	132430784	A	C	22	GENIC	homozygous	114990371
6	132431046	132431047	G	T	17	GENIC	homozygous	114990373
6	132431740	132431741	G	T	18	GENIC	homozygous	114990375
6	132432113	132432114	G	C	17	GENIC	homozygous	115081054
6	132432122	132432123	C	A	19	GENIC	homozygous	115081055
6	132432870	132432871	C	G	46	GENIC	homozygous	114990377
6	132432878	132432879	G	T	51	GENIC	homozygous	114990379
6	132433119	132433120	A	C	30	GENIC	homozygous	114990381
6	132433145	132433146	T	G	31	GENIC	possibly homozygous	114990383
6	132436424	132436425	G	A	15	GENIC	homozygous	114990384
6	132436821	132436822	C	T	11	GENIC	homozygous	114990388
6	132436866	132436867	C	A	17	GENIC	homozygous	115081056
6	132438307	132438308	T	G	29	GENIC	heterozygous	114990390