chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	50930323	50930324	T	C	18	GENIC	homozygous	53918512
7	50931361	50931362	C	T	24	GENIC	possibly homozygous	53918513
7	50931792	50931793	A	G	15	GENIC	possibly homozygous	53918515
7	50931984	50931985	A	G	26	GENIC	homozygous	53918516
7	50933289	50933290	T	C	26	GENIC	homozygous	53918521
7	50933553	50933554	G	-	12	GENIC	homozygous	53918522
7	50933933	50933934	T	C	17	GENIC	homozygous	53918527
7	50934983	50934984	T	-	14	GENIC	heterozygous	55141604
7	50935406	50935409	AAG	---	7	GENIC	possibly homozygous	53918532
7	50937334	50937335	G	T	11	GENIC	homozygous	53918535
7	50937739	50937740	G	C	10	GENIC	homozygous	53918536
7	50937740	50937741	G	T	10	GENIC	homozygous	53918537
7	50937745	50937746	G	GC	9	GENIC	homozygous	53918538
7	50937789	50937790	G	A	10	GENIC	homozygous	53918539
7	50937840	50937841	T	G	8	GENIC	homozygous	53918540
7	50937844	50937845	A	-	8	GENIC	homozygous	53918541
7	50938190	50938191	C	T	21	GENIC	homozygous	53918543
7	50938626	50938627	G	T	26	GENIC	homozygous	53918544
7	50941102	50941103	G	C	13	GENIC	homozygous	53918545