chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	113543918	113543918		T	42	GENIC	homozygous	143351077
7	113543931	113543932	G	A	45	GENIC	homozygous	143367062
7	113545399	113545400	A	T	58	GENIC	homozygous	138184529
7	113545400	113545401	T	G	58	GENIC	homozygous	138184530
7	113545401	113545402	C	T	57	GENIC	homozygous	143367063
7	113546829	113546830	G	A	40	GENIC	homozygous	143367064
7	113547147	113547148	C	T	40	GENIC	homozygous	143367065
7	113549034	113549035	C	T	59	GENIC	homozygous	143367066
7	113549432	113549433	T	C	64	GENIC	possibly homozygous	143367067
7	113551104	113551105	G	C	51	GENIC	homozygous	138184536
7	113548533	113548533		T	50	GENIC	homozygous	137975211
7	113552046	113552047	T		23	GENIC	possibly homozygous	403222748
7	113547683	113547684	A	G	36	GENIC	heterozygous	154482922
7	113551883	113551884	C	T	40	GENIC	homozygous	154482923
7	113547683	113547684	A		36	GENIC	heterozygous	403222745
7	113551883	113551884	C		40	GENIC	heterozygous	403222746
7	113552046	113552047	T	C	23	GENIC	heterozygous	403222747
7	113556013	113556014	T	C	61	GENIC	homozygous	138184558
7	113552976	113552977	C	T	55	GENIC	possibly homozygous	143367068
7	113553567	113553568	G	T	38	GENIC	homozygous	143367069
7	113554594	113554595	G	A	49	GENIC	homozygous	143367070
7	113556313	113556314	A	G	51	GENIC	homozygous	138184560
7	113556415	113556416	A	C	43	GENIC	homozygous	138184561
7	113558697	113558698	T	C	42	GENIC	homozygous	138184566
7	113558757	113558760	CTG		40	GENIC	homozygous	143351078
7	113558853	113558854	A	G	31	GENIC	homozygous	138184567
7	113560435	113560436	A	G	50	GENIC	homozygous	138184568
7	113560576	113560576		G	57	GENIC	homozygous	137975221
7	113562555	113562555		AAGCAGATAGGGGTAGGTTCAATGAGATGACCCT	47	GENIC	possibly homozygous	143351079
7	113562807	113562809	TC		57	GENIC	homozygous	143351080
7	113563068	113563069	T	G	60	GENIC	possibly homozygous	143367071
7	113563155	113563156	T	C	50	GENIC	homozygous	138184570