chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	56756878	56756879	A	G	44	GENIC	homozygous	112989889
15	56756996	56756997	G		35	GENIC	homozygous	133501139
15	56758369	56758370	C	T	37	GENIC	homozygous	112989890
15	56758667	56758668	A	C	36	GENIC	homozygous	112518306
15	56759672	56759673	T	A	31	GENIC	homozygous	112518312
15	56764231	56764232	A	G	66	GENIC	homozygous	112518316
15	56764971	56764972	A	G	56	GENIC	possibly homozygous	112518318
15	56765353	56765354	A	T	46	GENIC	homozygous	112518320
15	56765597	56765598	A	G	46	GENIC	homozygous	112518324
15	56766784	56766785	G	A	32	GENIC	homozygous	112989891
15	56768031	56768032	T	G	48	GENIC	homozygous	112518334
15	56768718	56768719	C	T	45	GENIC	homozygous	112518336
15	56759321	56759322	C	T	43	GENIC	homozygous	112879404
15	56768912	56768914	AA		35	GENIC	homozygous	129258899
15	56769618	56769619	A	G	50	GENIC	homozygous	112918491
15	56769939	56769939		AT	57	GENIC	homozygous	133281876
15	56770353	56770354	T	C	53	GENIC	homozygous	112689004
15	56770533	56770534	T	A	44	GENIC	homozygous	112918495
15	56771028	56771029	G	A	32	GENIC	homozygous	112989892
15	56771490	56771491	C	T	36	GENIC	homozygous	112989893
15	56772976	56772977	C	T	40	GENIC	homozygous	112918497
15	56773866	56773867	C	T	42	GENIC	homozygous	112918499
15	56773995	56773996	C	T	50	GENIC	homozygous	112918501
15	56774118	56774119	A	T	41	GENIC	homozygous	112918503
15	56774119	56774120	A	C	40	GENIC	homozygous	112918505
15	56774143	56774144	G	A	36	GENIC	homozygous	112989894
15	56774501	56774502	G	A	42	GENIC	homozygous	112918507
15	56775329	56775330	T	A	37	GENIC	homozygous	112989895
15	56775409	56775410	C	T	47	GENIC	homozygous	112989896
15	56775917	56775918	T	C	54	GENIC	homozygous	112918509
15	56776154	56776155	T	C	38	GENIC	homozygous	112689008
15	56775835	56775836	C	T	45	GENIC	homozygous	112989897