chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	136367144	136367145	A	T	42	GENIC	homozygous	118556380
6	136367145	136367146	T	C	42	GENIC	homozygous	115082209
6	136367508	136367509	G	A	38	GENIC	homozygous	114994881
6	136367802	136367803	T	C	34	GENIC	homozygous	114994882
6	136367888	136367889	C	T	29	GENIC	homozygous	114994883
6	136367891	136367892	T	C	28	GENIC	homozygous	114994884
6	136368176	136368177	T	G	41	GENIC	homozygous	114994885
6	136368755	136368756	G	T	24	GENIC	homozygous	114994886
6	136369393	136369394	G	A	47	GENIC	homozygous	114994887
6	136369727	136369728	T	C	39	GENIC	homozygous	114994888
6	136369954	136369955	A	G	41	GENIC	homozygous	114994889
6	136370078	136370079	T	C	23	GENIC	homozygous	114994890
6	136370100	136370101	T	C	22	GENIC	homozygous	114994891
6	136370105	136370106	G	A	22	GENIC	homozygous	114994892
6	136370522	136370523	T	C	33	GENIC	homozygous	114994893
6	136370550	136370551	G	A	33	GENIC	homozygous	118556381
6	136370591	136370592	G	A	28	GENIC	homozygous	114994894
6	136371131	136371132	G	A	31	GENIC	homozygous	114994895
6	136371165	136371166	A	G	27	GENIC	homozygous	114994896
6	136371817	136371818	C	T	35	GENIC	homozygous	114994898
6	136372055	136372056	T	C	42	GENIC	homozygous	114994899
6	136372300	136372301	C	T	24	GENIC	homozygous	114994900
6	136372655	136372656	G	A	28	GENIC	homozygous	114994901
6	136372927	136372928	G	A	28	GENIC	possibly homozygous	114994902
6	136372933	136372934	C	T	28	GENIC	possibly homozygous	114994903
6	136372999	136373000	A	G	23	GENIC	possibly homozygous	114994904
6	136373092	136373093	C	T	20	GENIC	homozygous	114994905
6	136380598	136380599	C	T	38	GENIC	homozygous	114994906