chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	73322658	73322661	TTT	---	42	GENIC	heterozygous	50831452
11	73322817	73322818	C	A	21	GENIC	heterozygous	51074362
11	73328740	73328741	T	A	34	GENIC	heterozygous	50831482
11	73332599	73332600	A	G	42	GENIC	heterozygous	50831493
11	73349163	73349164	A	T	18	GENIC	heterozygous	50831555
11	73352291	73352292	C	T	19	GENIC	heterozygous	51074423
11	73352489	73352490	A	C	62	GENIC	heterozygous	50831579
11	73353957	73353958	C	T	36	GENIC	heterozygous	51074434
11	73356614	73356615	G	C	55	GENIC	heterozygous	51074455
11	73359595	73359596	A	G	41	GENIC	heterozygous	50831600
11	73367732	73367733	G	A	46	GENIC	heterozygous	50831630
11	73367829	73367830	G	A	74	GENIC	heterozygous	50831631
11	73367862	73367863	A	G	83	GENIC	heterozygous	50831632
11	73368071	73368072	A	G	69	GENIC	heterozygous	50831633
11	73368104	73368105	A	C	51	GENIC	heterozygous	50831634
11	73368293	73368294	G	A	56	GENIC	heterozygous	51074494
11	73368401	73368402	T	TGGC	32	GENIC	heterozygous	50831636
11	73368590	73368591	C	T	51	GENIC	heterozygous	50831637
11	73374284	73374285	C	T	12	GENIC	heterozygous	51504360
11	73374389	73374390	C	T	28	GENIC	heterozygous	51504362