chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	177602944	177602945	C	T	15	GENIC	homozygous	62627725
1	177607561	177607562	A	T	14	GENIC	homozygous	60969180
1	177611912	177611913	G	A	20	GENIC	possibly homozygous	62627726
1	177612088	177612089	A	G	19	GENIC	possibly homozygous	60969184
1	177614481	177614482	C	T	25	GENIC	possibly homozygous	62627727
1	177615613	177615614	T	TG	2	GENIC	homozygous	61788540
1	177615656	177615657	T	C	11	GENIC	homozygous	62627728
1	177615797	177615798	T	C	19	GENIC	homozygous	60969198
1	177616646	177616647	A	G	20	GENIC	possibly homozygous	60969200
1	177618681	177618682	G	A	23	GENIC	possibly homozygous	62627729
1	177621036	177621037	C	-	8	GENIC	homozygous	60969210
1	177621195	177621196	G	-	15	GENIC	homozygous	60969212
1	177621691	177621692	C	T	22	GENIC	homozygous	60969214
1	177624055	177624056	G	T	11	GENIC	homozygous	62627730
1	177624883	177624884	C	T	30	GENIC	possibly homozygous	60969220
1	177625726	177625727	T	A	17	GENIC	possibly homozygous	62627731
1	177626672	177626673	T	G	17	GENIC	possibly homozygous	60969224
1	177628609	177628610	T	C	10	GENIC	possibly homozygous	60969229
1	177629638	177629639	C	T	10	GENIC	homozygous	62627732
1	177629731	177629732	C	T	10	GENIC	heterozygous	62627733
1	177633496	177633497	G	A	15	GENIC	homozygous	62627734