chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	95424737	95424738	C	T	18	GENIC	homozygous	110721854
2	95429257	95429258	G	T	28	GENIC	homozygous	109928579
2	95427336	95427337	T	C	32	GENIC	homozygous	110721855
2	95433493	95433494	A	G	27	GENIC	homozygous	109928591
2	95435997	95435998	A	C	24	GENIC	homozygous	110721857
2	95437662	95437663	G	A	14	GENIC	homozygous	110721858
2	95442211	95442212	G	T	37	GENIC	possibly homozygous	110721859
2	95444577	95444578	G	T	27	GENIC	homozygous	120286969
2	95445443	95445444	C	T	23	GENIC	homozygous	109928649
2	95448834	95448835	A	T	19	GENIC	homozygous	110721861
2	95459733	95459734	C	T	27	GENIC	homozygous	110721863
2	95459955	95459956	G	C	24	GENIC	homozygous	110721864
2	95460803	95460804	C	G	35	GENIC	homozygous	109928729
2	95461673	95461674	C	T	24	GENIC	homozygous	109928737
2	95461683	95461684	C	T	22	GENIC	homozygous	109928739
2	95461736	95461737	A	C	17	GENIC	possibly homozygous	109928741
2	95462489	95462490	G	A	22	GENIC	homozygous	110721866
2	95462774	95462775	A	G	21	GENIC	homozygous	110721867
2	95462901	95462902	A	C	27	GENIC	homozygous	110721869
2	95462906	95462907	A	T	28	GENIC	homozygous	110721870
2	95467033	95467034	C	T	7	GENIC	homozygous	110721872
2	95467991	95467992	C	T	13	GENIC	homozygous	109928749
2	95471397	95471398	C	T	19	GENIC	homozygous	110721874