chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92916654	92916655	G	GAA	13	GENIC	homozygous	49963536
13	92916726	92916727	G	T	27	GENIC	homozygous	50134802
13	92918750	92918751	C	-	10	GENIC	homozygous	49859766
13	92920146	92920147	A	G	21	GENIC	homozygous	49963559
13	92920691	92920692	T	A	37	GENIC	homozygous	49963561
13	92921027	92921028	A	G	31	GENIC	homozygous	49963562
13	92921287	92921291	AAAA	----	8	GENIC	homozygous	50134804
13	92925567	92925568	C	T	28	GENIC	homozygous	50134812
13	92921858	92921859	G	A	26	GENIC	homozygous	50134806
13	92922450	92922451	T	A	13	GENIC	homozygous	50134808
13	92924814	92924815	G	GAA	19	GENIC	possibly homozygous	50134810
13	92925912	92925913	A	G	33	GENIC	homozygous	50134814
13	92926268	92926269	T	C	28	GENIC	homozygous	50134816
13	92926613	92926614	A	G	19	GENIC	homozygous	50134818
13	92928185	92928189	CACC	----	24	GENIC	heterozygous	50134820
13	92928187	92928191	CCCC	----	15	GENIC	homozygous	50134822
13	92928206	92928207	T	C	20	GENIC	homozygous	49963568
13	92928239	92928240	A	C	22	GENIC	homozygous	49963569
13	92928780	92928781	G	A	18	GENIC	homozygous	49963570
13	92931040	92931041	C	A	30	GENIC	homozygous	49963572
13	92931125	92931126	C	T	24	GENIC	homozygous	50134824