chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	147744811	147744812	C	T	28	GENIC	heterozygous	113059386
4	147744842	147744843	A	G	33	GENIC	heterozygous	113059388
4	147744870	147744871	A	G	48	GENIC	heterozygous	113059390
4	147744884	147744885	A	G	47	GENIC	heterozygous	113059392
4	147744893	147744894	T	G	45	GENIC	heterozygous	113059394
4	147744902	147744903	T	G	45	GENIC	heterozygous	113059396
4	147745072	147745073	C	T	27	GENIC	homozygous	112874961
4	147745447	147745448	A	G	23	GENIC	homozygous	112874962
4	147745956	147745957	T	C	26	GENIC	homozygous	112874963
4	147746422	147746423	A	G	9	GENIC	homozygous	112874964
4	147746759	147746760	C	T	16	GENIC	homozygous	112874965
4	147746881	147746882	A	C	15	GENIC	homozygous	112874966
4	147747002	147747003	T	C	28	GENIC	homozygous	112874967
4	147747117	147747118	G	A	40	GENIC	homozygous	112874968
4	147747310	147747311	C	T	27	GENIC	homozygous	112874969
4	147748124	147748125	T	C	36	GENIC	homozygous	112874970
4	147748297	147748298	T	C	21	GENIC	homozygous	112874971
4	147749508	147749509	T	C	26	GENIC	homozygous	112874972
4	147749643	147749644	A	G	30	GENIC	homozygous	112874973
4	147749856	147749857	A	G	21	GENIC	homozygous	112874974
4	147750735	147750736	C	G	12	GENIC	homozygous	112874975
4	147751820	147751821	C	T	25	GENIC	homozygous	112874976
4	147752908	147752909	A	G	21	GENIC	homozygous	112874977
4	147753880	147753881	T	C	16	GENIC	possibly homozygous	112874978
4	147754040	147754041	C	A	36	GENIC	possibly homozygous	112874979
4	147754966	147754967	G	A	22	GENIC	homozygous	112874980
4	147756091	147756092	T	C	31	GENIC	homozygous	112874981