chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	9758998	9758999	G	T	28	GENIC	possibly homozygous	109631313
19	9759809	9759810	A		9	GENIC	homozygous	129582798
19	9759810	9759811	A	G	9	GENIC	homozygous	109631315
19	9761651	9761652	T	C	24	GENIC	homozygous	109631317
19	9761733	9761734	A	G	23	GENIC	homozygous	109631319
19	9761939	9761939		ATGTTGTCATGG	21	GENIC	homozygous	129582799
19	9762595	9762596	A	G	23	GENIC	homozygous	109631321
19	9762650	9762651	A	G	15	GENIC	homozygous	109631323
19	9763926	9763927	A	G	21	GENIC	homozygous	109631326
19	9764603	9764604	G	C	24	GENIC	homozygous	109631328
19	9764828	9764829	T	C	18	GENIC	homozygous	109631330
19	9765846	9765847	T		18	GENIC	possibly homozygous	129582800
19	9766187	9766188	G	A	15	GENIC	homozygous	109764355