chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157683346	157683347	T	C	43	GENIC	homozygous	112906898
4	157684282	157684282		GT	16	GENIC	possibly homozygous	132607640
4	157684503	157684504	C	T	26	GENIC	homozygous	113184577
4	157690378	157690379	A	G	40	GENIC	homozygous	112906906
4	157690797	157690798	C	T	40	GENIC	homozygous	112906908
4	157694518	157694519	C	T	47	GENIC	homozygous	113184582
4	157685531	157685532	A	C	46	GENIC	homozygous	113247249
4	157688614	157688614		T	33	GENIC	homozygous	128096227
4	157695892	157695893	A	G	41	GENIC	homozygous	113184583
4	157699868	157699869	A	T	36	GENIC	homozygous	113184584
4	157702801	157702801		G	36	GENIC	possibly homozygous	132607641
4	157703501	157703502	G	A	44	GENIC	possibly homozygous	113184585
4	157705347	157705348	A	G	48	GENIC	homozygous	113184586