chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	7304057	7304058	A	G	25	GENIC	homozygous	112049732
16	7304160	7304161	C	T	27	GENIC	homozygous	112228357
16	7304383	7304495	CTCTGTCTCTATCTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCC		15	GENIC	homozygous	132204413
16	7304586	7304586		CCCG	21	GENIC	homozygous	132204414
16	7305321	7305322	C	T	31	GENIC	homozygous	112049733
16	7306244	7306245	C	T	29	GENIC	homozygous	112049734
16	7306566	7306567	G		23	GENIC	homozygous	131743617
16	7306567	7306568	G	C	23	GENIC	homozygous	112049735
16	7306700	7306706	ACTGAC		31	GENIC	homozygous	131743618
16	7307518	7307519	G	C	31	GENIC	homozygous	112049736
16	7308478	7308479	A	C	33	GENIC	homozygous	112049737
16	7309007	7309008	G	A	28	GENIC	homozygous	112049738
16	7310221	7310222	A	G	29	GENIC	homozygous	112049739
16	7310637	7310637		CATATGTGTGTGTAGGC	32	GENIC	homozygous	131743620
16	7310940	7310941	T	C	33	GENIC	homozygous	112049740
16	7314297	7314298	T	A	33	GENIC	possibly homozygous	112049741
16	7315191	7315192	C	A	27	GENIC	homozygous	111927534
16	7314804	7314805	T	C	39	GENIC	homozygous	111927532