chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10025443	10025444	T	C	19	GENIC	homozygous	109632119
19	10025857	10025858	C	T	23	GENIC	homozygous	109764426
19	10025999	10026000	A	T	17	GENIC	homozygous	109632121
19	10026151	10026152	G	A	30	GENIC	homozygous	109632123
19	10028617	10028618	C	A	23	GENIC	homozygous	109632125
19	10028652	10028653	C	G	17	GENIC	homozygous	109632127
19	10028711	10028712	C	T	16	GENIC	homozygous	109850026
19	10028732	10028733	A	C	23	GENIC	homozygous	109799471
19	10028838	10028839	G	A	13	GENIC	homozygous	119596205
19	10029010	10029011	G	C	23	GENIC	homozygous	109912294
19	10029011	10029012	G	T	23	GENIC	homozygous	109912296
19	10029622	10029623	G	A	25	GENIC	homozygous	109632131
19	10030635	10030636	A	T	34	GENIC	homozygous	109632133
19	10032563	10032564	G	A	12	GENIC	homozygous	109632135
19	10033386	10033387	C	G	34	GENIC	possibly homozygous	119596206
19	10035040	10035041	C	T	29	GENIC	homozygous	109632137
19	10036225	10036226	A	G	46	GENIC	homozygous	109632139
19	10036349	10036350	G	A	23	GENIC	homozygous	109632143
19	10036412	10036413	G	A	26	GENIC	homozygous	109632145
19	10037689	10037690	G	C	26	GENIC	homozygous	109632147