chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	149413648	149413649	G	A	27	GENIC	homozygous	57517533
4	149413834	149413835	T	G	20	GENIC	homozygous	57517535
4	149414184	149414185	T	C	10	GENIC	heterozygous	57517537
4	149415196	149415197	C	T	13	GENIC	homozygous	57517539
4	149415245	149415246	T	-	6	GENIC	homozygous	57517541
4	149415868	149415869	A	G	5	GENIC	homozygous	57517543
4	149416020	149416021	T	C	19	GENIC	homozygous	57517549
4	149418788	149418789	A	G	17	GENIC	homozygous	57517553
4	149419103	149419104	G	A	8	GENIC	homozygous	57517555
4	149420199	149420200	G	A	12	GENIC	homozygous	57517557
4	149420584	149420585	C	CT	14	GENIC	possibly homozygous	57517565
4	149421912	149421913	T	G	17	GENIC	possibly homozygous	57517569
4	149422042	149422043	C	T	17	GENIC	homozygous	57517571
4	149422253	149422254	A	T	21	GENIC	homozygous	57517573
4	149422497	149422498	A	G	9	GENIC	homozygous	57517575
4	149425096	149425097	T	G	11	GENIC	homozygous	57517577
4	149425174	149425175	A	-	2	GENIC	homozygous	57517579
4	149425945	149425946	G	A	24	GENIC	homozygous	57517581
4	149426129	149426134	TTTTG	-----	7	GENIC	possibly homozygous	57517583
4	149426288	149426289	A	G	13	GENIC	heterozygous	57517585
4	149427447	149427448	C	A	5	GENIC	heterozygous	57517587