chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41969817	41969818	T	C	51	GENIC	homozygous	109702793
19	41971329	41971330	A	G	48	GENIC	homozygous	109702795
19	41973377	41973378	T	C	52	GENIC	homozygous	109702797
19	41973400	41973401	C	T	50	GENIC	homozygous	109702799
19	41973729	41973729		CC	9	GENIC	heterozygous	129609523
19	41973733	41973734	A	C	10	GENIC	heterozygous	109817347
19	41974392	41974393	G	C	62	GENIC	homozygous	109702801
19	41974911	41974912	T		39	GENIC	heterozygous	133449884
19	41974913	41974915	TA		40	GENIC	heterozygous	129609524
19	41980053	41980054	G	A	48	GENIC	homozygous	109702803
19	41980101	41980102	C	T	42	GENIC	homozygous	109702805
19	41980806	41980807	G	C	59	GENIC	homozygous	109702809
19	41983136	41983139	AGG		54	GENIC	homozygous	129609525
19	41985116	41985117	T	G	49	GENIC	homozygous	109702811
19	41985178	41985206	TTTTCCTGAAAACAAGAGCTTCCCTTTA		26	GENIC	homozygous	129609526
19	41985270	41985303	TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTC		13	GENIC	heterozygous	133787128
19	41986912	41986913	G	A	42	GENIC	homozygous	109702813
19	41989893	41989894	G	A	42	GENIC	homozygous	109702815
19	41990255	41990256	C	T	46	GENIC	homozygous	109702817
19	41990336	41990337	C	T	43	GENIC	homozygous	109702819
19	41974794	41974795	C	T	51	GENIC	homozygous	119630067