chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111013932	111013933	C	G	14	GENIC	homozygous	111673678
3	111014657	111014658	T	C	12	GENIC	homozygous	111673680
3	111015393	111015394	G	A	18	GENIC	homozygous	112292597
3	111016258	111016259	G	A	24	GENIC	homozygous	112292599
3	111017073	111017074	A	G	16	GENIC	homozygous	111673682
3	111017337	111017338	T	C	30	GENIC	homozygous	119702362
3	111017673	111017674	A	G	19	GENIC	homozygous	112139088
3	111017728	111017729	C	T	16	GENIC	homozygous	112292601
3	111018825	111018826	T	A	16	GENIC	homozygous	112292603
3	111020499	111020500	G	A	14	GENIC	homozygous	112292605
3	111020816	111020817	G	A	16	GENIC	homozygous	112292607
3	111021260	111021261	G	A	32	GENIC	homozygous	112292609
3	111021288	111021289	C	T	32	GENIC	homozygous	112292611
3	111021359	111021360	G	A	33	GENIC	homozygous	112292612
3	111021557	111021558	A	G	24	GENIC	homozygous	111673687
3	111021709	111021710	A	G	26	GENIC	homozygous	112292616
3	111017335	111017336	A		29	GENIC	homozygous	130907882
3	111017339	111017339		CT	30	GENIC	homozygous	130907883
3	111020834	111020836	CT		18	GENIC	homozygous	130907884
3	111021568	111021569	C	G	27	GENIC	homozygous	112292614