chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	160737395	160737396	T	TTCAC	4	GENIC	heterozygous	57540573
4	160745125	160745126	G	A	13	GENIC	possibly homozygous	58778448
4	160745299	160745300	A	G	18	GENIC	homozygous	57540581
4	160746495	160746496	A	G	15	GENIC	homozygous	57540583
4	160747151	160747152	A	C	15	GENIC	possibly homozygous	57540587
4	160749594	160749595	G	C	17	GENIC	homozygous	58173164
4	160752760	160752761	T	C	6	GENIC	homozygous	58778450
4	160753194	160753195	C	G	8	GENIC	possibly homozygous	58778452
4	160753419	160753420	A	G	9	GENIC	possibly homozygous	57540605
4	160754022	160754023	C	T	8	GENIC	possibly homozygous	58778454
4	160754071	160754072	T	C	8	GENIC	heterozygous	58778456
4	160754762	160754763	C	A	17	GENIC	possibly homozygous	57540609
4	160754846	160754847	T	C	13	GENIC	possibly homozygous	58778458
4	160754898	160754899	G	A	14	GENIC	heterozygous	58778460
4	160755360	160755365	AAAAC	-----	2	GENIC	homozygous	58778462
4	160755661	160755662	G	GT	6	GENIC	homozygous	58778464
4	160755803	160755804	G	A	8	GENIC	possibly homozygous	58778466
4	160755923	160755924	A	G	16	GENIC	possibly homozygous	58778468
4	160756607	160756608	C	T	9	GENIC	homozygous	58778470
4	160756881	160756882	C	CT	17	GENIC	homozygous	57540611
4	160757498	160757499	A	-	21	GENIC	possibly homozygous	58778472
4	160757811	160757812	C	T	21	GENIC	homozygous	58778474