chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111013932	111013933	C	G	21	GENIC	homozygous	111673678
3	111014657	111014658	T	C	23	GENIC	homozygous	111673680
3	111015393	111015394	G	A	28	GENIC	homozygous	112292597
3	111016258	111016259	G	A	36	GENIC	homozygous	112292599
3	111017073	111017074	A	G	29	GENIC	possibly homozygous	111673682
3	111017337	111017338	T	C	21	GENIC	homozygous	119702362
3	111017673	111017674	A	G	28	GENIC	homozygous	112139088
3	111017728	111017729	C	T	20	GENIC	homozygous	112292601
3	111018825	111018826	T	A	24	GENIC	possibly homozygous	112292603
3	111020499	111020500	G	A	23	GENIC	homozygous	112292605
3	111020816	111020817	G	A	19	GENIC	possibly homozygous	112292607
3	111021260	111021261	G	A	38	GENIC	homozygous	112292609
3	111021288	111021289	C	T	39	GENIC	homozygous	112292611
3	111021359	111021360	G	A	31	GENIC	homozygous	112292612
3	111021557	111021558	A	G	36	GENIC	homozygous	111673687
3	111021568	111021569	C	G	34	GENIC	homozygous	112292614
3	111021709	111021710	A	G	35	GENIC	homozygous	112292616