chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	179492471	179492471		T	20	GENIC	homozygous	147975381
4	179493528	179493529	T	C	39	GENIC	homozygous	137280631
4	179495037	179495037		T	19	GENIC	possibly homozygous	147975382
4	179496374	179496375	A	C	16	GENIC	homozygous	137280635
4	179496517	179496517		T	24	GENIC	homozygous	147975383
4	179497153	179497154	T	C	41	GENIC	homozygous	137280637
4	179496895	179496896	G	A	24	GENIC	homozygous	147991017
4	179497925	179497926	G	C	25	GENIC	homozygous	147991018
4	179493893	179493894	A	G	24	GENIC	homozygous	147991015
4	179496127	179496128	G	A	16	GENIC	homozygous	147991016
4	179499908	179499908		AATC	31	GENIC	homozygous	147975384
4	179500400	179500401	G	A	27	GENIC	homozygous	147991019
4	179500877	179500904	AAGAAAGAAAGAAAGAAAGAAAGAAAG		22	GENIC	homozygous	147975385
4	179500929	179500930	A	G	27	GENIC	homozygous	147991020
4	179503221	179503222	T	A	22	GENIC	homozygous	137280641
4	179503760	179503761	C	T	26	GENIC	possibly homozygous	147991021
4	179504819	179504820	G	A	14	GENIC	homozygous	147991022
4	179504866	179504867	G	T	2	GENIC	homozygous	147991023
4	179505217	179505218	G	A	26	GENIC	homozygous	147991024
4	179505525	179505526	C	T	30	GENIC	homozygous	147991025
4	179505536	179505537	A	G	33	GENIC	homozygous	137280643
4	179506341	179506342	A	G	29	GENIC	homozygous	147991026
4	179507795	179507796	C	T	29	GENIC	homozygous	147991027
4	179507948	179508052	AAGACATCATAGGGGGGGAGGGGGATGTTTGCCCGGAAACCGGGAAAGGGAATAACACTCGAAATGTATATAAGAAATACTCAAGTTAATAAAAAAAAAAAAAA		17	GENIC	homozygous	147975386
4	179508070	179508071	A		20	GENIC	homozygous	147975387
4	179508827	179508828	G	A	28	GENIC	homozygous	147991028
4	179509949	179509950	T	C	22	GENIC	homozygous	147991029
4	179510706	179510707	G	A	28	GENIC	homozygous	147991030
4	179511045	179511046	A	G	31	GENIC	homozygous	147991031
4	179504943	179504944	A		8	GENIC	homozygous	136933115