chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	177606208	177606209	C	A	33	GENIC	homozygous	61788536
1	177606695	177606696	G	A	39	GENIC	homozygous	61788538
1	177607561	177607562	A	T	43	GENIC	possibly homozygous	60969180
1	177612088	177612089	A	G	31	GENIC	homozygous	60969184
1	177615613	177615614	T	TG	23	GENIC	homozygous	61788540
1	177616646	177616647	A	G	52	GENIC	homozygous	60969200
1	177621036	177621037	C	-	32	GENIC	homozygous	60969210
1	177621195	177621196	G	-	34	GENIC	homozygous	60969212
1	177621691	177621692	C	T	31	GENIC	homozygous	60969214
1	177623302	177623303	A	G	23	GENIC	heterozygous	61788542
1	177623313	177623314	T	TAC	17	GENIC	heterozygous	61788544
1	177624513	177624514	G	A	48	GENIC	possibly homozygous	61788546
1	177624883	177624884	C	T	43	GENIC	homozygous	60969220
1	177626672	177626673	T	G	34	GENIC	homozygous	60969224
1	177627588	177627589	C	CTT	17	GENIC	homozygous	60969227
1	177628609	177628610	T	C	41	GENIC	homozygous	60969229
1	177628848	177628849	A	AAC	26	GENIC	possibly homozygous	60969231
1	177634886	177634887	C	T	4	GENIC	homozygous	61788548