chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	12211488	12211489	T	A	32	GENIC	homozygous	115044968
6	12211497	12211498	G	T	30	GENIC	homozygous	115044969
6	12211543	12211544	C	T	33	GENIC	homozygous	115044970
6	12211607	12211608	A	G	30	GENIC	homozygous	115044971
6	12211684	12211685	C	T	23	GENIC	homozygous	115044972
6	12211701	12211702	T	G	27	GENIC	homozygous	118552371
6	12211702	12211703	G	T	28	GENIC	homozygous	118552372
6	12211799	12211800	A	G	28	GENIC	homozygous	115044973
6	12211804	12211805	A	G	28	GENIC	homozygous	115044974
6	12211850	12211851	T	C	31	GENIC	homozygous	115044975
6	12212476	12212477	G	A	32	GENIC	homozygous	115044976
6	12212521	12212522	T	G	25	GENIC	possibly homozygous	115044977
6	12212576	12212577	T	C	23	GENIC	homozygous	115044978
6	12212758	12212759	T	C	33	GENIC	homozygous	115044979
6	12212775	12212776	G	A	28	GENIC	homozygous	115044980
6	12212899	12212900	C	T	37	GENIC	homozygous	115044981
6	12213222	12213223	T	G	15	GENIC	homozygous	115044982
6	12213234	12213235	G	T	14	GENIC	homozygous	115044983
6	12213842	12213843	T	C	4	GENIC	homozygous	115044984
6	12213878	12213879	A	G	13	GENIC	homozygous	115044985
6	12214132	12214133	T	C	22	GENIC	homozygous	115044986