chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38152997	38152998	A	C	33	GENIC	possibly homozygous	109814190
19	38156567	38156568	T	C	7	GENIC	homozygous	132239275
19	38156581	38156581		CCTCCC	6	GENIC	homozygous	132234888
19	38159394	38159395	A		38	GENIC	homozygous	132234889
19	38159801	38159802	C	T	46	GENIC	homozygous	109814192
19	38160462	38160464	CC		41	GENIC	homozygous	132234890
19	38161513	38161514	G	A	40	GENIC	homozygous	109814194
19	38166923	38166924	C	T	55	GENIC	homozygous	109814198
19	38168378	38168378		A	23	GENIC	homozygous	132234891
19	38168652	38168653	A		38	GENIC	possibly homozygous	132234892
19	38169611	38169612	C	T	51	GENIC	homozygous	109814200
19	38170236	38170237	T		55	GENIC	homozygous	132234893
19	38170370	38170371	T	C	40	GENIC	homozygous	109814202
19	38170635	38170636	A	G	60	GENIC	homozygous	109814204
19	38172208	38172209	C	T	46	GENIC	homozygous	109814212
19	38171271	38171272	T	C	38	GENIC	homozygous	109814206
19	38171285	38171286	T	A	39	GENIC	homozygous	109814208
19	38171440	38171441	T	C	41	GENIC	homozygous	109814210
19	38156588	38156589	G	C	6	GENIC	homozygous	110065546
19	38156591	38156592	A	C	6	GENIC	homozygous	110065548
19	38156597	38156598	A	C	7	GENIC	homozygous	119629301
19	38165224	38165225	G	T	19	GENIC	homozygous	119629303
19	38168372	38168373	A	T	25	GENIC	homozygous	119665321
19	38172568	38172569	G	T	55	GENIC	homozygous	109814214
19	38172688	38172688		T	20	GENIC	homozygous	132234894
19	38175124	38175125	A	G	44	GENIC	homozygous	109814216
19	38175326	38175327	G	A	54	GENIC	homozygous	109814218
19	38176349	38176350	T	C	44	GENIC	homozygous	109814220
19	38178047	38178048	T	C	44	GENIC	homozygous	109814222
19	38179027	38179028	T	G	50	GENIC	homozygous	109814224