chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	143636500	143636501	G	C	25	GENIC	homozygous	60878162
1	143636635	143636636	A	G	14	GENIC	possibly homozygous	60878163
1	143637033	143637035	TC	--	11	GENIC	homozygous	61532289
1	143637327	143637328	A	G	18	GENIC	possibly homozygous	60878164
1	143638171	143638172	G	T	27	GENIC	possibly homozygous	60878165
1	143638739	143638740	T	C	33	GENIC	possibly homozygous	60878166
1	143639346	143639347	T	-	4	GENIC	homozygous	61532290
1	143639607	143639608	G	T	8	GENIC	possibly homozygous	60878167
1	143639723	143639724	C	A	8	GENIC	possibly homozygous	60878168
1	143639768	143639769	C	T	10	GENIC	homozygous	60878169
1	143640457	143640458	T	A	22	GENIC	possibly homozygous	60878171
1	143640743	143640744	G	A	11	GENIC	possibly homozygous	60878172
1	143641097	143641098	G	C	23	GENIC	possibly homozygous	60878173
1	143641293	143641294	G	A	27	GENIC	homozygous	60878174
1	143641811	143641812	G	A	15	GENIC	possibly homozygous	60878175
1	143643209	143643210	T	C	22	GENIC	possibly homozygous	60878177
1	143643351	143643352	T	C	12	GENIC	heterozygous	60878178
1	143643560	143643561	T	C	7	GENIC	homozygous	60878179
1	143643612	143643613	T	C	16	GENIC	homozygous	60878180
1	143643771	143643772	T	C	14	GENIC	homozygous	60878181
1	143643805	143643806	G	A	19	GENIC	possibly homozygous	60878182
1	143643937	143643938	C	T	15	GENIC	homozygous	60878183
1	143644346	143644347	T	TA	2	GENIC	heterozygous	60878184
1	143645960	143645961	A	G	8	GENIC	possibly homozygous	60878185
1	143646194	143646195	G	A	7	GENIC	heterozygous	61675254
1	143646237	143646238	C	CCCA	4	GENIC	homozygous	61532291