chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	143632446	143632447	C	CT	26	GENIC	possibly homozygous	61675242
1	143632835	143632836	G	GGT	7	GENIC	heterozygous	62162898
1	143632835	143632836	G	GGTGT	7	GENIC	heterozygous	62162900
1	143636500	143636501	G	C	26	GENIC	homozygous	60878162
1	143636635	143636636	A	G	29	GENIC	homozygous	60878163
1	143637327	143637328	A	G	21	GENIC	homozygous	60878164
1	143638171	143638172	G	T	28	GENIC	homozygous	60878165
1	143638739	143638740	T	C	32	GENIC	homozygous	60878166
1	143639607	143639608	G	T	36	GENIC	homozygous	60878167
1	143639723	143639724	C	A	27	GENIC	homozygous	60878168
1	143639768	143639769	C	T	34	GENIC	homozygous	60878169
1	143639924	143639925	G	GTGTTT	10	GENIC	homozygous	60878170
1	143640457	143640458	T	A	25	GENIC	homozygous	60878171
1	143640743	143640744	G	A	20	GENIC	homozygous	60878172
1	143641097	143641098	G	C	27	GENIC	homozygous	60878173
1	143641293	143641294	G	A	37	GENIC	homozygous	60878174
1	143641811	143641812	G	A	27	GENIC	homozygous	60878175
1	143641982	143641983	C	CT	4	GENIC	homozygous	60878176
1	143643209	143643210	T	C	35	GENIC	homozygous	60878177
1	143643351	143643352	T	C	34	GENIC	homozygous	60878178
1	143643560	143643561	T	C	39	GENIC	homozygous	60878179
1	143643612	143643613	T	C	27	GENIC	homozygous	60878180
1	143643771	143643772	T	C	38	GENIC	homozygous	60878181
1	143643805	143643806	G	A	38	GENIC	homozygous	60878182
1	143643937	143643938	C	T	22	GENIC	homozygous	60878183
1	143643989	143643990	T	TTTAA	15	GENIC	homozygous	61675252
1	143644346	143644347	T	TA	27	GENIC	homozygous	60878184
1	143644785	143644786	G	A	29	GENIC	homozygous	61903013
1	143646194	143646195	G	A	23	GENIC	homozygous	61675254
1	143646236	143646237	C	CA	19	GENIC	homozygous	61903014
1	143646237	143646238	C	CCCCCA	19	GENIC	homozygous	61903015